Method for Identifying the Function of a Gene

ABSTRACT

Described is a method for determining the function of a gene. This method involves determining the amount of transcript for each of a set of candidate genes in samples taken from different phenotypic and/or genotypic states of an organism and determining the amount of each of a plurality of metabolites in different samples taken from the same states as those mentioned above. Subsequently, the data obtained is analyzed by suitable mathematical methods in order to identify a transcript and metabolites which correlate in the different states, thereby identifying a transcript corresponding to a gene which influences the amount of metabolites in the organism. Furthermore described is a method for identifying a gene which is capable of modifying the amount of a metabolite in an organism and to a method for identifying a metabolite which is capable of modifying the amount of a transcript in an organism. Likewise, uses of the genes and metabolites identified in the aforementioned methods are described.

The present invention relates to a method for determining the function of a gene. This method involves determining the amount of transcript for each of a set of candidate genes in samples taken from different phenotypic and/or genotypic states of an organism and determining the amount of each of a plurality of metabolites in different samples taken from the same states as those mentioned above. Subsequently, the data obtained is analyzed by suitable mathematical methods in order to identify a transcript and one or more metabolites which correlate in the different states, thereby identifying a transcript corresponding to a gene which influences the amount of these one or more metabolites in the organism. The invention furthermore relates to a method for identifying a gene which is capable of modifying the amount of a metabolite in an organism and to a method for identifying a metabolite which is capable of modifying the amount of a transcript in an organism. Likewise, the present invention relates to uses of the genes and metabolites identified in the aforementioned methods.

Since the advent of genetic engineering, many techniques have become available that allow the purposeful and specific modification of the transcript level of a given gene. This may lead to either an increase or to a decrease of the transcript level in a so-manipulated cell. Corresponding techniques have been described for many biological systems comprising various classes of prokaryptes and eukaryotes. The change in the transcript level may be effected transiently or, such as in the case of corresponding genetically modified organisms, constitutively.

However, until today, it cannot be reliably foreseen what effect the modified transcript level of a given gene has on the phenotype of the organism. The term “phenotype” refers herein to any possible detectable property of an organism, in particular including the amount of a polypeptide or, further downstream in the reaction path of gene expression, the amount of a metabolite in a cell. The uncertainty about the effect of a modification of the transcript level is mainly due to the complexity of the events that contribute to the expression of a certain phenotype which often involves a redundancy of the various gene expression and regulatory mechanisms, in particular when eukaryotes, and there especially higher eukaryotes such as mammals, plants or insects, are considered. For instance, up to now, one cannot reliably predict whether a significant reduction of a transcript, e.g. by antisense or RNA interference approaches, will effectively lead to a decrease of the corresponding protein activity in the cell. However, if already at the protein level the effect of a transcript reduction is uncertain, the more unpredictable is then the outcome of such a measure at the level of metabolites. Thus, when it is for instance the task to increase or decrease the amount of a certain metabolite, such as a nutritibonally relevant compound in a plant, the scientists often fail to reach this goal or only achieve a minor success (see for instance DellaPenna, Science 285 (1999), 375-379). Here, the effect of a modified transcription of a gene that is involved in a biochemical pathway is often compensated by feedback control mechanisms or alternative pathways, as it beforehand could not have been foreseen. Thus, those who attempt to reach such goals are normally faced with an enormous extent of trial and error. Such experimental approaches are usually costly and time-consuming since they often involve the production of genetically modified organisms. Thus, there is a need for methods that allow it to more effectively apply the well-established techniques of modifying transcript levels in order to modify the metabolite composition of an organism.

Taking the inverse view, there is likewise a need for effector molecules that are capable of specifically modifying the transcription rate of a gene. This applies particularly to pathogenic conditions and diseases where, for instance due to a mutation, a certain gene is aberrantly over- or underexpressed.

In the post-genomic era, scientists working in medical and biological disciplines are confronted with the need of assigning functions to genes which have been identified in the course of genome sequencing. Based on this and following the aim to more comprehensively understand the regulatory processes in a cell, systems biology has evolved in the recent years (Kitano, 2002; Ideker, 2001; Oltvai, 2002). This field refers to multi-parallel analyses of a multitude of parameters of a given biological system at a range of different molecular levels following a systematic perturbation of the biological system.

The starting point of systems biology can be seen in the genomic research making use of the advanced technologies allowing the sequencing of enkaryotic genomes (see e.g. Arabidopsis and Human Genome Sequencing, 2000 & 2001) and the analysis of the expression level of complete genomes or large proportions thereof (i.e. transcriptomic analyses) (Lockhart, 1996). However, it is becoming increasingly clear that a wide range of post-translational factors bear functional importance in the cell as well. Thus, the development of strategies to allow similar comprehensive studies of the protein and metabolite complements (proteomics (Shevchenko, 1996) and metabolomics (Fiehn, 2000; Roessner, 2001)) of the cell have begun, but still at a relatively early stage. Despite the well-known connectivity between the molecules described by the transcriptomic, proteomic and metabolomic approaches, only a few studies have been described where it was tried to correlate parameters across the various levels (Ideker, 2001; Gygi, 1999; Futcher, 1999). In particular, approaches where transcriptomic data is directly correlated with metabolomic data has to date not yet been described.

In view of the above explanations, it is clear that there is a need for techniques allowing an improved deployment of transcription modification to achieve a deliberate change of metabolite composition in a biological system.

Thus, the technical problem underlying the present invention is the provision of means and methods that render it possible to modify the level of one or more metabolites in a given organism in a more reliable and predictable manner.

This technical problem is solved by the provision of the embodiments as characterized in the claims.

Accordingly, the present invention relates to a method for determining the function of a gene comprising

-   -   (a) determining the amount of transcript for each of a set of         candidate genes in two or more samples from an organism, wherein         the samples correspond to different phenotypic and/or genotypic         states of said organism;     -   (b) determining the amount of each of a plurality of metabolites         present in two or more samples corresponding to the same states         as in (a);     -   (c) analysing by suitable mathematical methods the data obtained         in steps (a) and (b) in order to identify a transcript and at         least one metabolite the amounts of which significantly         correlate in the different states,         said transcript corresponding to a gene having a function that         influences the amount of said metabolite(s) in said organism.

The method of the invention is based on experiments by which it was surprisingly possible to find significant correlations between the amount of a transcript and the amount of a metabolite when different developmental stages of wild-type potato tubers and transgenic potato tubers are compared (see Example 2). Interestingly, it has been observed that the amount of one transcript may correlate significantly with the amount of more than one metabolite. Likewise, it has been seen that the amount of one metabolite may correlate significantly with the amount of more than one transcript. The observed correlations provide the information that the gene corresponding to the identified transcript may have a function that influences the amount of the one or more metabolites in the organism under investigation. Correspondingly, it can be expected that this gene is a promising target for an intervention that leads to a modified transcript amount of this gene in the corresponding organism if it is intended to modify the amount of said one or more metabolites. Furthermore, on the other hand, it is likewise conceivable that a metabolite the amount of which significantly correlates with the amount of one or more transcripts, or a structurally related compound exercising essentially similar effects, can be an effector molecule useful for modifying the amount of said transcript in the corresponding organism.

Specifically, in the experiments described in Example 2, 518 out of the 23715 transcript-metabolite pairs analysed exhibited significant correlations, whereby 329 correlations were positive and 189 negative. Some of the observed correlations confirmed interrelationships between gene expression and metabolite level that were already known. This provides the proof that the method of the invention works and gives reasonable results. This refers for instance to the strong negative correlation observed between sucrose and sucrose transporter expression (FIG. 2 a) that has previously been described by Vaughn (2002). The same holds true for the strong positive correlation between 4-amino butyric acid and glutamate decarboxylase isoform I (FIG. 2 b) previously described by Facchini (2000). Other observed correlations can at least retrospectively be explained based on the function of the encoded polypeptide. For instance, the metabolite may be a substrate, product or intermediate in a biochemical pathway in which the polypeptide participates. Examples for this are depicted in FIGS. 2 c to 2 f. Most interestingly, the analysis carried out according to the method of the invention also provided significant correlations which by no means could have been foreseen. This refers for example to the correlations shown in FIGS. 2 k to 2 p referring, e.g. to correlations between nutritionally relevant metabolites and transcription factors (see Example 2). It is believed that such new correlations may have a great potential for biotechnological applications in which it is the goal to modify the metabolite composition by genetic means or where effector compounds are needed for modifying the expression of a specific gene. In particular, the newly identified transcript-metabolite correlations are envisaged to present a powerful tool for the rapid identification of candidate genes which can then be tested by further experimentation for their value regarding applicability. The approach presented herein has not been described before.

By the method of the invention, it is possible to determine the function of a gene. The method involves the above-mentioned steps (a) to (c) by which a significant correlation between the amount of one or more transcripts with the amount of one or more metabolites in different states of an organism is determined. Such a correlation provides the information that, in the organism under investigation, a gene corresponding to the (or a) transcript of this correlation may have the function that it influences the amount of the one or more metabolites to which it correlates.

In connection with the method of the invention, the term “gene” refers to the conventional meaning of this term in the field of molecular genetics. In particular, a gene whose function is determined by applying the method of the invention is a nucleic acid molecule which, under suitable conditions, is transcribed and, if the gene encodes a polypeptide, translated. A “coding sequence” is that part of a gene which encodes an amino acid sequence.

The term “function of a gene” means any possible function that a gene may have as long as this function influences the amount of one or more metabolites in the organism under investigation. Typically the function of the gene will be exerted by the gene product, in most cases a polypeptide, that it encodes. The term “function of a gene” embraces the possibility that, for the gene in question, already a function is known, and that, by applying the method of the invention, a novel function will be revealed. Therefore, the term “determining the function of a gene” may in particular mean determining one of the functions of a gene, preferably an additional function of a gene of which one or more functions are already known. If for example, a gene is known to encode a transcription factor, the novel function may be to influence the amount of a nutritionally relevant or essential metabolite. It may be possible that the known function is directly or indirectly involved in the novel function, but that this causality was hitherto not known. In the given example, this would mean that, for instance, the transcription factor is responsible for the synthesis of an enzyme that participates in the biosynthesis of the metabolite.

The term “influences the amount of said metabolite(s) in said organism” means any kind of causal relationship between the activity of a gene or its gene product and the amount of a metabolite in the organism. Such an influence may for example be a more or less direct influence in that the gene encodes an enzyme which participates in the biosynthesis or the metabolization or degradation of the metabolite. On the other hand, the influence may be indirect such as that the gene regulates the activity or the amount of an enzyme which participates in the biosynthesis or the metabolization or degradation of the metabolite.

It is preferred that the gene of which the function is determined by the method of the invention encodes an enzyme, a regulatory protein, a transport protein or a transcription factor.

The term “set of candidate genes” refers to a plurality of genes the amount of transcript of which is determined in step (a). The method of the invention requires that a selection is made of the genes to be analyzed, thereby taking into account a number of factors. These factors include the availability of sequence information of the genes rendering it feasible to obtain specific and significant data on the transcript amount. It is certainly favorable if it is known that the candidate gene is transcribed in the organism of which the samples are taken. Furthermore, experimental restrictions as to the feasibility to produce suitable probes for the respective gene may play a role. Also, the genes to be analyzed in step (a) may be pre-selected by the individual user according to certain predictions on the gene function or requirements concerning for example the intended use of the gene of which a novel function is sought. For instance, in the experiments underlying the present invention, the candidate genes were selected among genes encoding enzymes involved in the primary metabolism and transcription factors. Among these in turn, genes were selected from available tomato EST libraries. In particular, each candidate gene corresponds to one so-called Tentative Consensus (TC) sequence, each being created by assembling ESTs into virtual transcripts. TCs contain full or partial cDNA sequences (ESTs) obtained by classical methods. TCs contain information on the source library and the abundance of ESTs and in many cases represent full-length transcripts. Alternative splice forms are built into separate TCs. To create TCs, CAP3, a DNA sequence assembly program, was used (Huang, X. and Madan, A. (1999) CAP3: A DNA Sequence Assembly Program. Genome Research, 9: 868-877).

The tomato genes used are annotated as described by Van der Hoeven (Plant Cell 14 (2002), 1441-1456). At least two EST clones were selected for microarray construction for each analyzed candidate gene. This example for selecting candidate genes may be adapted by the individual user of the present invention according to his needs. In particular, it may be recommendable to select more than one, if not more than two or even more than three EST clones or corresponding probe molecules being specific for one candidate gene for constructing a microarray or an equivalent device for analyzing the amount of transcripts in step (a) of the method of the invention. Here the methodologies according to the state of the art, such as described in Aharoni (Plant Mol. Biol. 48 (2002), 99-118), may be applied.

In general the number of genes which are analyzed in step (a) should be as big as possible in order to be able to obtain as many as possible correlations between transcripts and metabolites.

In a preferred embodiment, a set of at least 20, preferably of at least 50, more preferably at least 100, and even more preferred of at least 200 genes is used in step (a).

The term “transcript” refers to the RNA that is produced upon transcription of each candidate gene which may be in particular mRNA or also pre-mRNA, i.e. the primary transcript of a gene or a premature processed form thereof. The “amount of transcript” determined in step (a) is the quantity of the transcript in the sample and may for example be expressed in the form amount per fresh or dry weight of the sample. The amount of transcript depends on several factors, however mainly on the transcription rate of the corresponding gene and on the RNA degradation rate.

In step (a), the transcript amount may be determined by applying any suitable technique available to the person skilled in the art. Preferred are techniques that allow the parallel quantification of a plurality of transcripts, especially if data retrieval can be carried out partially or fully automatically. In the field of transcriptome analysis corresponding suitable techniques have been described which mainly focus on the use of DNA chips or microarrays (see for example Aharoni (loc. cit.), Colebatch, 2002 and Thimm, 2001).

In a preferred embodiment, the determination of the amount of transcript is performed as described in the Examples.

In a preferred embodiment of the method of the invention, for determining the amount of transcripts, probes are used that are homologous with respect to the organism of which the samples are taken.

This means that each probe, at least in the region where it is aimed that hybridization takes place, is essentially complementary to the sequence of the transcript of the respective candidate genes. Preferably, the complementary sequence of the probe is identical with the complement of said transcript over the corresponding stretch. However, the use of homologous probes is not a mandatory requirement. It is also possible to use heterologous probes, i.e. for instance derived from a different species than that of the organism under investigation. In this case, however, one should take care that each probe reliably hybridizes with the respective transcript.

The amount of transcript of the candidate genes and the amount of metabolites is determined from two or more samples from an organism, wherein the samples correspond to different phenotypic and/or genotypic states of said organism. The term “organism” refers to any living matter that is capable of gene expression. In particular, “living matter” may be one or more cells, a tissue, an organ or a complete organism such as a plant or an animal. The living matter may be in a naturally occurring form or in a man-made form such as in a cultured form, e.g. cell culture, protoplast culture, tissue culture or the like or in the form of a genetically modified organism. In connection with metabolite determination, the term “organism” also includes the direct environment of the living matter, wherein the “direct environment” is characterized by the presence of a metabolite or a gene product produced by said living matter. This gene product may for example influence the metabolite content in the environment of the cell. The direct environment may for example be the extracellular space around a cell, the apoplast, the cell wall, the interstitial space or a culture medium. Furthermore, the metabolite sample may be taken from a certain part of the organism as for example from certain cellular compartments such as plastids, mitochondria, the nucleus, vacuole etc.

The samples analyzed in steps (a) and (b) are taken from different phenotypic and/or genotypic states of said organism. This is explained by the fact that correlations within the transcript and metabolite composition can only be found if the organism is in different states, whereby these states must be connected with differences in the transcript content and in the metabolite content of the organism. It is the idea behind the present invention that a correlation between a transcript and a metabolite may indicate a causal interrelatedness between the two compounds. Therefore, it is envisaged that, in accordance with the correlation observed, the artificial modification of the amount of one compound may lead to a modification of the amount of the other compound. Thereby, the first compound may be either the transcript or the metabolite.

The term “phenotypic state” refers to differences in the phenotype of the organism under investigation. “Phenotype” means any kind of feature that can be detected and which is not a feature of the genome. Such phenotypic states may for example be visually identified such as a morphological or anatomical difference like they can be observed at different developmental stages. Phenotypic states may likewise manifest themselves by the composition of chemical compounds or the occurrence of a disease. Thus, the phenotypic states may be a healthy state in comparison to one or more pathogenic states, different stages of a pathogenicity or an uninfected versus one or more infected organisms.

The term “genotypic state” reflects differences in the genome of the organism. Thus, if the samples are taken from different genotypic states of an organism, the term “organism” specifically refers to organisms according to the definition given above which belong to the same taxonomic unit, but which differ in at least one genetic trait. Specifically, the “taxonomic unit” is a genus, preferably a species, and more preferably an even lower taxonomic rank such as a race, variety, cultivar, strain, isolate, population or the like. Most preferably, the taxonomic rank is an isogenic line with variance in only a limited number, preferably three, more preferably two genetic traits and most preferably one genetic trait, whereby “genetic tirait” refers to a chromosomal region, a gene locus or, as it is preferred, to a gene. Typically, differences in the genotypic state can be differences between a wild-type organism and one or more corresponding mutant or transgenic organisms or between different mutant or transgenic organisms. A certain genotypic state may be stable or transient as is the case with transduced or transfected cells for instance containing a plasmid, phage or viral vector. Advantageously, organisms of different genotypic state are analyzed when they are in the same developmental stage.

It is immediately clear that the terms “phenotypic” and “genotypic” states may overlap. In particular, normally a genotypic state, if the differing genetic trait(s) is/are expressed in the organism, lead(s) to a difference in the phenotype.

According to the above explanations, in a preferred embodiment of the method of the invention, the different phenotypic and/or genotypic states are different developmental stages, taxonomic units, wild-type and mutant or transgenic organisms, infected and uninfected states, diseased and healthy states or different stages of a pathogenicity.

For each phenotypic and/or genotypic state of the organism, samples are taken in order to determine the amount of the transcripts and the metabolites in these samples.

The term “sample” encompasses any amount of material taken from the organism that is susceptible to the method of the invention. For instance, a sample can be fresh material such as a tissue explant, a body fluid or an aliquot from a bacterial or cell culture, preferably deprived of the culture medium, that may be directly subjected to extraction. On the other hand, samples may also be stored for a certain time period, preferably in a form that prevents degradation of the transcripts and metabolites in the sample. For this purpose, the sample may be frozen, for instance in liquid nitrogen, or lyophilized.

The samples may be prepared according to methods known to the person skilled in the art and as described in the literature. In particular, the preparation should be carried out in a way that the respective compounds to be analyzed are not degraded during the extraction in order to prevent a falsification of the determination in steps (a) and (b). The samples for transcription analysis may for example be prepared according to procedures described in Logemann (1987). The samples for metabolite analysis may for example be prepared according to procedures described in Roessner (2000).

Advantageously, the sample preparation involves the employment of suitable methods in order to remove detection-disturbing compounds from the transcripts (RNA) and/or the metabolites prior to determining the amounts of said transcripts and/or metabolites in the samples. This refers in particular to detection-disturbing compounds which are carbohydrates or other compounds that may disturb identification and quantification of RNA. Routinely, compounds that may disturb the detection of RNA or metabolites are removed by suitable techniques known to the skilled practitioner if such a removal improves the quality and significance of the detection (i.e. the determination of the amounts of said compounds in the sample). For example, it has been shown that the presence of carbohydrates disturbs the detection of RNA by microarrays and that the removal of the carbohydrates from the sample may significantly improve the quality of the detected signals.

In a preferred embodiment of the method of the invention, the amount of transcripts and the amount of metabolites is each determined from the same sample.

This preferred embodiment is based on a technology described in PCT/EP03/00196 and in Fiehn (Eur. J. Biochem. 270 (2003), 579-588). The method described therein provides data useful for quantitatively analyzing metabolites, proteins and/or RNA in a biological source material, whereby said analysis involves suitable statistical evaluation and correlation analysis on the data obtained. In this method, extracting, identifying and quantifying of at least two compound classes of the group consisting of metabolites, proteins and RNA are each determined from one sample. Accordingly, in the preferred embodiment of the method of the present invention, steps (a) and (b) are carried out by applying the corresponding teachings of PCT/EP03/06196. In a particularly preferred embodiment, steps (a) and (b) are performed by (i) extracting the metabolites from the respective sample with at least one solvent or mixture of solvents; and (ii) extracting the RNA from the remainder of the sample after step (i). Thereby, it is a further option that metabolites may additionally be extracted from the yet undissolved remaining cellular material contained in the sample after (ii). Preferably, extraction is carried out by using a mixture of solvents that comprises at least one highly polar solvent, at least one less polar solvent and at least one lipophilic solvent. Thereby, the use of a mixture of solvents comprising water, methanol and chloroform is particularly preferred. More preferably, this mixture of solvents contains water, methanol and chloroform in the approximate proportion by volume of 1:2.5:1. Advantageously, the extraction in step (i) is carried out at a temperature between −60° C. and +4° C.

The term “metabolite” refers to any substance within an organism of which a sample useful for applying the method of the invention can be taken and for which techniques for determining the amount are available. According to the invention, nucleic acid molecules are not within the meaning of “metabolite”. Preferably, the metabolites addressed by the present invention have a low molecular weight, i.e. for instance not more than 4000 Da, preferably not more than 2000 Da, more preferably not more than 1000 Da. Typically, the metabolites to be analyzed may belong to the following, however non-limiting list of compounds: carbohydrates (e.g. sugars, oligo- and polysaccharides such as polyglucans as for example starch or polyfructans), sugar alcohols, amines, polyamines, amino alcohols, aliphatics, aliphatic alcohols, amino acids, lipids, fatty acids, fatty alcohols, organic acids, organic phosphates, organic or anorganic ions, nucleotides, sugar nucleotides, sterols, terpenes, terpenoids, flavons and flavonoids, glucosides, carotenes, carotenoids, cofactors, ascorbate, tocopherol and vitamins.

In a particularly preferred embodiment, the metabolites to be analyzed comprise sugars, sugars alcohols, organic acids, amino acids, ascorbate, tocopherol, fatty acids, vitamins and/or polyamines.

The number and selection of metabolites analysed in step (b) depends on the question for which kind of metabolites a correlation with transcripts is aimed to be determined. Moreover, this depends on the availability of suitable techniques for determining the amount of the respective metabolite, wherein “determining” means identifying and quantifying.

Accordingly, in a preferred embodiment of the invention, the amount of at least 20, more preferably at least 50, still more preferably at least 100, even more preferably at least 150 and most preferably at least 200 or even at least 300 metabolites is determined in step (b).

The determination of the amount of metabolites of interest can be done according to well-known techniques known in the prior art and familiar to the person skilled in the art. Preferably, techniques are applied that allow the identification and quantification in one step and, advantageously, are suited to record the respective metabolites contained in the sample in a comprehensive manner.

For example, the metabolites may be identified and quantified using gas chromatography/mass spectrometry (GC/MS), liquid chromatography/mass spectrometry (LC/MS), NMR or FT-IR or combinations thereof. Further useful methods include LC/UV, refractory index determination, the use of radioactivity in connection with suitable methods known to the skilled person, thin layer chromatography (TLC), capillary electrophoresis (CE), CE/UV, CE/laser induced fluorescence (LIF), fluorescence detection, electrochemical detection (i.e. colorimetry), direct injection MS, flow injection MS, MS/MS, MS/MS/MS, and further combinations of MS steps (MSn), fourier transform ion mass spectrometry (FT/MS), and gel permeation chromatography (GPC). If appropriate, any of the above methods may be combined.

An exemplary non-biased analysis is described in Fiehn (2000). In this study, of different plant mutants, 326 distinct compounds (ranging from primary polar metabolites to sterols) were detected and relatively quantified, including both identified and non-identified compound's by applying a GC/MS analysis. Another example of a GC/MS analysis that can be applied in the method of the invention has been described by Roessner (2001), who used it for comprehensively studying the metabolism in potato tubers. Alternatively, metabolite data can be obtained by extended chromatographic analysis such as described by Tweeddale (1998) where, after growing wild type and mutant E. coli strains in minimal media and 14C-labelled glucose, 70 metabolites could be separated using two dimensional thin layer chromatography. The relative quantification of metabolites was carried out by radioactive detection.

In step (c), the data obtained in steps (a) and (b) are analyzed by applying suitable mathematical methods in order to identify a transcript and at least one metabolite the amounts of which significantly correlate in the different phenotypic and/or genotypic states.

The term “analyzed by applying suitable mathematical methods” refers to any mathematical analysis method that is suited to further process the quantitative data obtained in steps (a) and (b) in a way that significant correlations between transcripts and metabolites can be ascertained. These data represent the amount of the analyzed compounds present in each sample either in absolute terms (e.g. weight or moles per weight sample) or in relative terms (i.e. normalized to a certain reference quantity). Usually normalized data is used for performing correlation analyses. Normalization may involve the representation of the amount of an examined compound at each state by setting the figure in relation to one reference value determined at one specific state. Normalization may furthermore involve the correction of background levels and the combination of the transcript and the metabolite data sets into a single data sheet. Corresponding mathematical methods and computer programs are known to the skilled person. Examples include SAS, SPSS, systatR, R and Matlab. As the next step, the statistically pre-processed data may be subjected to a pairwise correlation analysis. Here series of pairs of data points from the analyzed compounds are looked at for correlation, whether positive or negative, for instance by using the Pearson's correlation coefficient.

In a preferred embodiment, the mathematical analysis of the method of the invention furthermore involves network analysis. Network analysis aims at finding out higher order interplays of multiple factors on the basis of pairwise correlation data. By taking several data sets each obtained from one sample, correlations between metabolites and transcripts as well as among these classes of compounds can be analysed in order to derive information about the network regulation of biological systems, e.g. upon genetic or environmental perturbation. The analysis of pairwise correlations in particular between metabolites and transcripts allows to establish links between regulatory and metabolic networks and the computation of general properties such as connectivity for both types of networks.

A comprehensive overview of methods for quantitatively analyzing data obtained according to the method of the invention including principle component analysis, “snapshot analysis”, Pearson correlation analysis, mutual information and network analyses can be found in Fiehn (2001).

According to the present invention, a significant correlation between the amount of a transcript and the amount of a metabolite in the different states, whereby the candidate genes may be pre-selected or non-selected, can be determined by a non-parametric Spearman's rank order correlation analyzis. Rank order correlation appears to be preferable to other methods because transcript and metabolite levels may be correlated in a non-linear manner. In particular, in a first step, for all possible transcript and metabolite pairs Spearman correlation coefficients may be calculated. Subsequently, the correlation coefficients may be compared with a Spearman Rank significance table for specific parameters (P=0.01). This approach has also been taken in the experiments described in Example 2. The value r_(s) is the result of the Spearman correlation coefficient calculation. The formula for the Rank (Spearman) Correlation Coefficient is

$r_{s} = {1 - \frac{6{\sum d^{2}}}{n\left( {n^{2} - 1} \right)}}$

In a preferred embodiment, step (c) of the method of the invention comprises the steps

-   -   (i) determining transcripts the amount of which differs         significantly between the samples of (a); and     -   (ii) determining metabolites the amount of which differs         significantly between the samples of (b);         wherein the data obtained for the transcripts and the         metabolites determined in steps (i) and (ii), respectively, are         analyzed by suitable mathematical methods in order to identify         said transcript and metabolite(s) the amounts of which         significantly correlate in the different states.

In this embodiment, first those transcripts and metabolites are determined the amount of which shows significant differences between the analyzed states of the organism. Corresponding statistical analysis methods and applicable software are known to the person skilled in the art and described in the literature. This may for example be done as it is described in Example 1. On the so-pretreated data, the analysis for finding pairwise correlations between transcripts and metabolites may be performed as described above. Preferably, only the transcripts and metabolites showing significant differences as determined in steps (i) and (ii), respectively, may be used for the correlation analysis. This may have the advantage of saving computational and other capacities.

It is the result of the method of the invention to identify a transcript in step (c) that significantly correlates with at least one metabolite in the different states. This finding gives an indication that the gene corresponding to this transcript has a function that influences the amount of said metabolite(s) in said organism. The term “gene corresponding to a transcript” refers to the gene from which the transcript is transcribed. The gene can be identified according to conventional techniques common to the molecular biologist. The term “function that influences the amount of a metabolite” has already been defined further above.

In a further aspect, the present invention relates to a method for identifying a gene which is capable of modifying the amount of a metabolite in an organism comprising steps (a) to (c) of the aforementioned method for determining the function of a gene, wherein said transcript identified in step (c) corresponds to a gene being capable of modifying the amount of said metabolite(s) identified in step (c).

The term “gene capable of modifying the amount of a metabolite in an organism” refers to a gene having the function to influence the amount of a metabolite in the organism as it can be determined by the corresponding method described above. As a consequence, it is contemplated that an exogenously induced alteration of the expression of this gene as compared to the normal wild-type gene expression in the organism under the same developmental and environmental conditions will lead to a significant modification of the amount of said metabolite in the organism as compared to the amount of the metabolite in the corresponding organism with the expression of said gene not being altered.

Thus, when a correlation between a transcript and a metabolite has been revealed by the method of the invention, a gene corresponding to this transcript can be made the target of a specific alteration of its gene expression if it is intended to deliberately modify the amount of the metabolite. In this context, the term “altered gene expression” refers to any measures that lead to an altered amount of the transcript of said gene in the organism. Primarily encompassed are measures that modify the transcription rate or the stability of the transcript RNA. However, if the gene encodes a polypeptide, measures are also encompassed that modify the translation rate, the activity of the encoded gene product or post-translational modifications of the polypeptide resulting in a modified activity of the gene product. Depending on whether the correlation is positive or negative, an increased gene expression may lead to an increase or a decrease of the amount of the metabolite in the organism. Accordingly, a decreased gene expression may lead to a decrease or an increase of the metabolite in the organism. This effect can be employed, for example, in order to produce useful plants having an increased content in a nutritionally valuable metabolite such as a vitamin or having a reduced content in a undesirable metabolite such as a compound being responsible for allergic reactions. Likewise, the effect can be used in gene therapeutical approaches in order to increase or decrease a certain metabolite in a specific tissue or organ.

Often it will be necessary that the modification of the particular metabolite is not accompanied by the modification of other metabolites which might evoke undesirable side effects. In such a case, a gene can be selected for modification which does not show significant correlations with other metabolites.

Various methods for exogenously inducing an alteration of the expression of a specific gene are known and described in the literature that can be applied when a gene has been identified that is capable of modifying the amount of a metabolite in an organism.

An increase of gene expression may for example be achieved by over-expressing the corresponding gene product from a gene construct introduced into said organism by applying conventional methods such as those described in Sambrook. (2001) and Gassen (1999). However, the state of the art provides further methods for achieving an increased gene expression. For example, the corresponding endogenous gene may be modified at its natural location, e.g. by homologous recombination, for example by positively affecting the promoter activity. Applicable homologous recombination techniques (also known as “in vivo mutagenesis”) are known to the person skilled in the art and are described in the literature. One such technique involves the use of a hybrid RNA-DNA oligonucleotide (“chimeroplast”) which is introduced into cells by transformation (TIBTECH 15 (1997), 441-447; WO95/15972; Kren, Hepatology 25 (1997), 1462-1468; Cole-Strauss, Science 273 (1996), 1386-1389).

A reduction of gene expression may be achieved by different techniques described in the prior art. These include but are not limited to antisense, ribozyme, co-suppression, RNA interference, expression of dominant negative mutants, antibody expression and in vitro mutagenesis approaches. All of them include the introduction of a suitable nucleic acid molecule into a cell. Such a foreign nucleic acid molecule is present in cells of a correspondingly treated organism, but absent from the cells of the corresponding source organism. Thereby encompassed are nucleic acid molecules, e.g. gene sequences, which differ from the corresponding nucleic acid molecule in the source organism by at least one mutation (substitution, insertion, deletion, etc. of at least one nucleotide), wherein such a mutation inhibits the expression of the affected gene or reduces the activity of the gene product. Furthermore encompassed by the term “foreign” are nucleic acid molecules which are homologous with respect to the source organism but are situated in a different chromosomal location or differ, e.g., by way of a reversed orientation for instance with respect to the promoter.

In principle, the nucleic acid molecule to be introduced in accordance with the present embodiment may be of any conceivable origin, e.g. eukaryotic or prokaryotic. It may be from any organism which comprises such molecules. Furthermore, it may be synthetic or derived from naturally occurring molecules by, e.g., modification of its sequence, i.e. it may be a variant or derivative of a naturally occurring molecule. Such variants and derivatives include but are not limited to molecules derived from naturally occurring molecules by addition, deletion, mutation of one or more nucleotides or by recombination. It is, e.g., possible to change the sequence of a naturally occurring molecule so as to match the preferred codon usage of the target organism. It is preferred that the nucleic acid molecule introduced into the organism has to be expressed in order to exert its reducing effect upon gene expression of the target gene. The term “expressed” means that such a nucleic acid molecule is at least transcribed and, for some embodiments, also translated into a protein. Preferred examples of such nucleic acid molecules relate to those embodiments wherein a reduced gene expression is achieved by an antisense, co-suppression, ribozyme or RNA interference effect or by the expression of antibodies or other suitable polypeptides capable of specifically reducing the activity of the encoded gene product or by the expression of a dominant-negative mutant. These methods are further explained in the following.

In particular, gene expression may be reduced by using nucleic acid molecules encoding an antisense RNA or directly by using antisense RNA, said antisense RNA being complementary to transcripts of the gene the expression of which is to be reduced. Thereby, complementarity does not signify that the RNA has to be 100% complementary. A low degree of complementarity may be sufficient as long as it is high enough to inhibit the gene expression. The transcribed RNA is preferably at least 90% and most preferably at least 95% complementary to the transcript of the gene. In order to cause an antisense effect during the transcription the antisense RNA molecules have a length of at least 15 bp, preferably a length of more than 100 bp and most preferably a length or more than 500 bp, however, usually less than 2000 bp, preferably shorter than 1500 bp. For example, for plants, exemplary methods for achieving an antisense effect are described by Muller-Röber (EMBO J. 11 (1992), 1229-1238), Landschütze (EMBO J. 14 (1995), 660-666), D'Aoust (Plant Cell 11 (1999), 2407-2418) and Keller (Plant J. 19 (1999), 131-141). Likewise, an antisense effect may also be achieved by applying a triple-helix approach, whereby a nucleic acid molecule complementary to a region of the respective gene is designed according to the principles for instance laid down in Lee (Nucl. Acids Res. 6 (1979), 3073); Cooney (Science 241 (1998), 456) or Dervan (Science 251 (1991), 1360).

A similar effect as with antisense techniques can be achieved by applying RNA interference (RNAi). Thereby, the formation of double-stranded RNA leads to an inhibition of gene expression in a sequence-specific fashion. More specifically, in RNAi constructs, a sense portion comprising the coding region of the gene to be inactivated (or a part thereof, with or without non-translated region) is followed by a corresponding antisense sequence portion. Between both portions, an intron not necessarily originating from the same gene may be inserted. After transcription, RNAi constructs form typical hairpin structures. The RNAi technique may be carried out as described by Smith (Nature 407 (2000), 319-320), Marx (Science 288 (2000), 1370-1372) or Elbashir (Nature 411 (2001), 428-429).

Furthermore, DNA molecules can also be employed which, during their expression lead to the synthesis of an RNA which reduces the expression of the gene to be inactivated due to a co-suppression effect. The principle of co-suppression as well as the production of corresponding DNA sequences is precisely described, for example, in WO 90/12084. Such DNA molecules preferably encode an RNA having a high degree of homology to transcripts of the target gene. It is, however, not absolutely necessary that the coding RNA is translatable into a protein. The principle of the co-suppression effect is known to the person skilled in the art and is, for example, described in Jorgensen, Trends Biotechnol. 8 (1990), 340-344; Niebel, Curr. Top. Microbiol. Immunol. 197 (1995), 91-103; Flavell, Curr. Top. Microbiol. Immunol. 197 (1995), 43-36; Palaqui and Vaucheret, Plant. Mol. Biol. 29 (1995), 149-159; Vaucheret, Mol. Gen. Genet. 248 (1995), 311-317; de Bome, Mol. Gen. Genet. 243 (1994), 613-621 and in other sources.

Likewise, ribozymes which specifically cleave transcripts of the gene to be inactivated can be used. Ribozymes are catalytically active RNA molecules capable of cleaving RNA molecules at a specific target sequence. There are various classes of ribozymes. For practical applications aiming at the specific cleavage of the transcript of a certain gene, use is preferably made of the group I intron ribozyme type or of ribozymes exhibiting the so-called “hammerhead” motif as a characteristic feature. By means of recombinant DNA techniques, the specific recognition of the target RNA molecule may be modified by altering the sequences flanking the hammerhead motif. By base pairing with sequences in the target molecule, the flanking sequences determine the position at which cleavage of the target molecule takes place. Since the sequence requirements for an efficient cleavage are low, it is in principle possible to develop specific ribozymes for practically each desired RNA molecule. In order to produce nucleic acid molecules encoding a ribozyme which specifically cleaves the transcript of the gene to be inactivated, for example, a DNA sequence encoding a catalytic domain of a ribozyme is bilaterally linked with DNA sequences which are complementary to sequences of the transcript. Sequences encoding the catalytic domain may for example be the catalytic domain of the satellite DNA of the SCMo virus (Davies, Virology 177 (1990), 216-224 and Steinecke, EMBO J. 11 (1992), 1525-1530) or that of the satellite DNA of the TobR virus (Haseloff and Gerlach, Nature 334 (1988), 585-591); The expression of ribozymes in order to decrease the activity of certain proteins in cells is known to the person skilled in the art and is, for example, described in EP-B1 0 321 201. The expression of ribozymes in plant cells is for example described in Feyter (Mol. Gen. Genet. 250 (1996), 329-338).

Furthermore, nucleic acid molecules encoding antibodies specifically recognizing the polypeptide encoded by the gene to be inactivated or specific fragments or epitopes of such a polypeptide can be used for inhibiting the gene expression of said gene. These antibodies can be monoclonal antibodies, polyclonal antibodies or synthetic antibodies as well as fragments of antibodies, such as Fab, Fv or scFv fragments etc. Monoclonal antibodies can be prepared, for example, by the techniques as originally described in Köhler and Milstein (Nature 256 (1975), 495) and Galfré (Meth. Enzymol. 73 (1981) 3), which comprise the fusion of mouse myeloma cells to spleen cells derived from immunized mammals. Furthermore, antibodies or fragments thereof to the aforementioned polypeptide can be obtained by using methods which are described, e.g., in Harlow and Lane “Antibodies, A Laboratory Manual”, CSH Press, Cold Spring Harbor, 1988. In plants, expression of antibodies or antibody-like molecules can be achieved by methods well known in the art. These include the expression of, for example, full-size antibodies (Düring, Plant. Mol. Biol. 15 (1990), 281-293; Hiatt, Nature 342 (1989), 469-470; Voss, Mol. Breeding 1 (1995), 39-50), Fab-fragments (De Neve, Transgenic Res. 2 (1993), 227-237), scFvs (Owen, Bio/Technology 10 (1992), 790-794; Zimmermann, Mol. Breeding 4 (1998), 369-379; Taviadoraki, Nature 366 (1993), 469-472; Artsaenko, Plant J. 8 (1995), 745-750) and variable heavy chain domains (Benvenuto, Plant Mol. Biol. 17 (1991), 865-874) have been successfully expressed in tobacco, potato (Schouten, FEBS Lett. 415 (1997), 235-241) or Arabidopsis, reaching expression levels as high as 6.8% of the total protein (Fiedler, Immunotechnology 3 (1997), 205-216).

Moreover, also nucleic acid molecules encoding peptides or polypeptides capable of reducing the activity of the polypeptide encoded by the gene to be inactivated other than antibodies can be used in the present context. Examples of suitable peptides or polypeptides that can be constructed in order to achieve the intended purpose can be taken from the prior art and include, for instance, binding proteins such as lectins.

In addition, nucleic acid molecules encoding a mutant form of the polypeptide encoded by the gene to be inactivated can be used to interfere with the activity of the wild-type protein. Such a mutant form preferably has lost its biological activity and may be derived from the corresponding wild-type protein by way of amino acid deletion(s), substitution(s), and/or additions in the amino acid sequence of the protein. Mutant forms of such proteins may show, in addition to the loss of the hydrolytic activity, an increased substrate affinity and/or an elevated stability in the cell, for instance, due to the incorporation of amino acids that stabilize proteins in the cellular environment. These mutant forms may be naturally occurring or, as is preferred, genetically engineered mutants.

It is also possible that the nucleic acid molecule, the presence of which in the genome of an organism leads to a reduction of gene expression, does not require its expression to exert its reducing effect on gene expression. Correspondingly, preferred examples relate to methods wherein this effect is achieved by in vivo mutagenesis or by the insertion of a heterologous DNA sequence in the target gene. The term “in vivo mutagenesis”, relates to methods where the sequence of the gene to be inactivated is modified at its natural chromosomal location such as for instance by techniques applying homologous recombination. This may be achieved by using a hybrid RNA-DNA oligonucleotide (“chimeroplast”), as described above.

The term “insertion of a heterologous DNA sequence” refers to DNA sequences which can be inserted into the target gene via appropriate techniques other than in vivo mutagenesis. The insertion of such a heterologous DNA sequence may be accompanied by other mutations in the target gene such as the deletion, inversion or rearrangement of the sequence located at the insertion site. In connection with preparing transgenic plants, this embodiment includes randomly introducing a heterologous DNA sequence into the respective plant genome, thereby generating a pool, i.e. a plurality, of transgenic plants having a genome into which the heterologous DNA sequence is randomly spread over various chromosomal locations. This generation of transgenic plants is followed by selecting those transgenic plants out of the pool which show the desired genotype, i.e. an inactivating insertion in the target gene and/or the desired phenotype, i.e. a reduced activity of the polypeptide encoded by the target gene and/or a modified amount of the metabolite which correlates with the transcript of said gene.

Suitable heterologous DNA sequences that can be taken for such an approach are described in the literature and include for instance vector sequences capable of self-integration into the host genome or mobile genetic elements. Particularly preferred in this regard are T-DNA or transposons which are well-known, to the person skilled in the art from so-called tagging experiments used for randomly knocking out genes in plants. The production of such pools of transgenic plants can for example be carried out as described in Jeon (Plant J. 22 (2000), 561-570) or Parinov (Curr. Op. Biotechnol. 11 (2000), 157-161).

Another example of insertional mutations that may result in gene silencing includes the duplication of promoter sequences which may lead to a methylation and thereby an inactivation of the promoter (Morel, Current Biology 10 (2000), 1591-1594).

Furthermore, it is immediately evident to the person skilled in the art that the above-described approaches, such as antisense, ribozyme, co-suppression, in-vivo mutagenesis, RNAi, expression of antibodies, other suitable peptides or polypeptides or dominant-negative mutants and the insertion of heterologous DNA sequences, can also be used for reducing the expression of a gene that encodes a regulatory protein such as a transcription factor that controls the expression of the gene to be inactivated. It is also evident from the above descriptions any of the above-mentioned approaches can be combined in order an effective reduction of gene expression of the target gene.

In yet another aspect, the present invention refers to a method for identifying a metabolite which is capable of modifying the amount of a transcript in an organism comprising steps (a) to (c) of the aforementioned method for determining the function of a gene, wherein a metabolite identified in step (c) is a candidate for a metabolite being capable of modifying the amount of said transcript identified in step (c).

The term “metabolite capable of modifying the amount of a transcript in an organism” refers to a metabolite the amount of which significantly correlates with said transcript in the different states of the organism as it can be determined by performing steps (a) to (c) of the above-described method for determining the function of a gene. It is thus contemplated that an exogenously induced alteration of the amount of the metabolite as compared to the normal amount of the metabolite in the organism under the same developmental and environmental conditions may lead to a significant modification of the amount of the transcript in the organism as compared to the amount of the transcript in the corresponding organism with the amount of said metabolite not being altered. Thus, when a correlation between a metabolite and a transcript has been revealed by the method of the invention, a metabolite or a thereto structurally related compound can be regarded as a candidate for a compound that may modify the expression of the gene corresponding to this transcript.

The term “candidate” reflects that the metabolite identified in step (c) may not necessarily be causative for the observed differences of the correlated transcript in the different states of the organism under investigation. Thus, it may be required that the identified metabolite be further tested for the property of being capable of modifying the amount of the transcript in an organism. For this purpose, gene expression assays may be conducted according to methods known in the prior art as for instance described in Sambrook (2001) and Gassen (1999). For example, the amount of the respective transcript may be detected for the organism to which a certain amount of the candidate metabolite is added in comparison with a corresponding organism at the same conditions to which no metabolite is added. As already mentioned above, such a candidate may also be a compound which is structurally related to the specific metabolite and which has a similar effect on the transcript level as the metabolite.

It is envisaged that the method of the present embodiment may for example provide novel starting points for developing therapeutically useful agents that may be used for ameliorating an aberrant over- or under-expression of a gene in a patient who suffers from a genetic disease.

Generally, most of the metabolites that occur in nature may be synthesized chemically or by microorganisms or by a combination of these two possibilities and often are commercially available. Correspondingly, modifications to a metabolite compound may be introduced according to methods of organic chemistry and biochemistry known in the art. Compounds being structurally related with a metabolite thus produced may be tested for their activity of modifying the amount of a transcript with which said metabolite correlates according gene expression assays known in the art, as mentioned above.

In this context, an “alteration of the amount of a metabolite” may on the one hand mean an increase of this amount in the organism. This may be achieved by the addition of this metabolite or of a structurally related compound having a similar effect on the transcript level to be modified to the organism. Alternatively, other methods for increasing the amount of a certain metabolite in an organism known in the prior art may be used as well such as measures that indirectly lead to an increase of the metabolite in the organism, e.g. by influencing the biosynthesis or degradation of the metabolite. On the other hand, the “alteration of the amount of a metabolite” may be a reduction of this amount in the organism.

For administering a metabolite or a structurally related compound having a corresponding activity, said metabolite or structurally related compound may be formulated in a composition.

If for example administration is meant for plants the composition may be composed in the form of a plant protection composition, wherein the metabolite or the structurally related compound may be formulated by conventional means commonly used for the application of, for example, herbicides or pesticides. For example, certain additives known to those skilled in the art such as stabilizers or substances which facilitate the uptake by the plant cell, plant tissue or plant may be used as for example harpins, elicitins, salicylic acid (SA), benzol(1,2,3)thiadiazole-7-carbothioic acid (BTH), 2,6-dichloro isonicotinic acid (INA), jasmonic acid (JA) or methyljasmonate.

If for example administration is meant for mammals or corresponding mammalian cells or tissues, the composition may be composed in the form of a pharmaceutical composition and may further comprise a pharmaceutically acceptable carrier and/or diluent. The composition may furthermore contain substances that stabilize or facilitate the uptake of the metabolite or compound by the cells. Examples of suitable pharmaceutical carriers are well known in the art and include phosphate buffered saline solutions, water, emulsions, such as oil/water emulsions, various types of wetting agents, sterile solutions etc. Compositions comprising such carriers can be formulated by well known conventional methods. These pharmaceutical compositions can be administered to the subject at a suitable dose. Administration of the suitable compositions may be effected by different ways, e.g., by intravenous, intraperitoneal, subcutaneous, intramuscular, topical, intradermal, intranasal or intrabronchial administration. The dosage regimen will be determined by the attending physician and clinical factors. As is well known in the medical arts, dosages for any one patient depends upon many factors, including the subject's size, body surface area, age, the particular compound to be administered, sex, time and route of administration, general health, and other drugs being administered concurrently. A typical dose can be, for example, in the range of 0.001 to 1000 μg (or of nucleic acid for expression or for inhibition of expression in this range); however, doses below or above this exemplary range are envisioned, especially considering the aforementioned factors. Generally, the regimen as a regular administration of the pharmaceutical composition should be in the range of 1 μg to 10 mg units per day. If the regimen is a continuous infusion, it should also be in the range of 1 μg to 10 mg units per kilogram of body weight per minute, respectively. Progress can be monitored by periodic assessment.

Compositions may be administered locally or systemically. Preparations for parenteral administration include sterile aqueous or non-aqueous solutions, suspensions, and emulsions. Examples of non-aqueous solvents are propylene glycol, polyethylene glycol vegetable oils such as olive oil, and injectable organic esters such as ethyl oleate. Aqueous carriers include water, alcoholic/aqueous solutions, emulsions or suspensions, including saline and buffered media. Parenteral vehicles include sodium chloride solution, Ringer's dextrose, dextrose and sodium chloride, lactated Ringer's, or fixed oils. Intravenous vehicles include fluid and nutrient replenishers, electrolyte replenishers (such as those based on Ringer's dextrose), and the like. Preservatives and other additives may also be present such as, for example, antimicrobials, anti-oxidants, chelating agents, and inert gases and the like.

Often it will be necessary that the modification of the particular transcript level induced by the correlated metabolite is not accompanied by the modification of the amount of other transcripts which might evoke undesired side effects. In such a case, a metabolite can be selected which does not'show significant correlations with other transcripts.

Furthermore, the present invention relates to the use of a gene the function of which has been determined by the above-described method for determining the function of a gene, of a nucleic acid molecule comprising the coding sequence of said gene or a fragment or derivative of said coding sequence showing said function or of a polypeptide encoded by said gene or nucleic acid molecule for applying said function. With the method of the invention, it is possible to elucidate gene functions that have not been thought of before. Therefore, the present invention also refers to the use of the genes for applying the function that has been identified by the method of the invention.

In the experiments underlying this invention, several new correlations between transcript level and metabolite level have been revealed. Accordingly, the present invention refers in particularly preferred embodiments to the uses of the genes corresponding to these transcripts for applying the newly revealed functions each of which involves influencing the amount of the respective metabolite, preferably in a plant, especially in potato, more specifically in potato tuber.

In particular, these uses are evident for the person skilled in the art from the following transcript-metabolite correlations (see also Example 2):

-   -   (1) a positive correlation of tryptophan with the beta-2chain of         tryptophan synthase (FIG. 2 c);     -   (2) a positive correlation of tyrosine with the beta-2 chain of         tryptophan synthase (FIG. 2 d);     -   (3) a positive correlation of serine with ornithine         carbamoyltransferase (FIG. 2 e);     -   (4) a positive correlation of cysteine with ornithine         carbamoyltransferase (FIG. 2 f);     -   (5) a positive correlation of fructose-6-phosphate with         aminotransferase (FIG. 2 g);     -   (6) a positive correlation of glucose-6-phosphate with         aminotransferase which correlates with both fructose-6-phosphate         and glucose-6-phosphate (FIG. 2 h);     -   (7) a positive correlation of spermidine with glutamate         decarboxylase isoform I (FIG. 2 i);     -   (8) a positive correlation of tyrosine with glutamate         decarboxylase isoform I (FIG. 2 j);     -   (9) a negative correlation of ascorbate with a homologue of the         clock gene CONSTANS (FIG. 2 k);     -   (10) a negative correlation of tocopherol with succinyl CoA         synthetase (FIG. 2 l);     -   (11) a positive correlation of lysine with the transcription         factor WRKY6 (FIG. 2 m);     -   (12) a positive correlation of lysine with         S-adenosyl-L-methionine synthetase (FIG. 2 n);     -   (13) a positive correlation of lysine with ornithine         carbamoyltransferase (FIG. 2 o);     -   (14) a negative correlation of lysine with caffeoyl-CoA         O-methyltransferase (FIG. 2 p);     -   (15) a negative correlation of sucrose with osmotic         stress-induced zinc-finger protein;     -   (16) a positive correlation of 4-aminobutyric acid with osmotic         stress-induced zinc-finger protein; and     -   (17) a positive correlation of tryptophan with osmotic         stress-induced zinc-finger protein.

Since most molecular biological applications do not use a gene sequence (in particular if it contains one or more introns), but the coding sequence or fragments or derivatives thereof, the uses of the present inventions are not limited to the genes identified according to the methods of the invention, but also refer to nucleic acid molecules comprising the coding sequence of said gene or a fragment or derivative of said coding sequence showing said function.

The terms “nucleic acid molecule” and “coding sequence of a gene” refer to the conventional meaning of these terms as they are familiar to the skilled person. The term “nucleic acid molecule” furthermore encompasses molecules which, in addition to said coding sequence, comprise additional sequences useful for the intended uses. Such additional nucleotide sequences may in particular be additional coding sequences fused to the aforementioned coding sequence, said additional coding sequence for example encoding a tag facilitating easy purification of the encoded fusion protein, a stabilizing moiety inhibiting degradation of the fusion protein or targeting signal sequences. Furthermore, such additional nucleotide sequences may be expression control sequences operably linked to the coding sequence or vector sequences allowing the propagation of the nucleic acid molecule in a suitable host. Corresponding construction manuals for nucleic acid molecules are known to the skilled person and described in the literature (see e.g. Sambrook (2001) and Gassen (1999)).

The term “fragment of said coding sequence showing said function” refers to fragments of the coding sequence of the gene that has the function of influencing the amount of a metabolite to which the transcript of said gene shows a correlation, whereby the fragment when expressed in a corresponding organism shows a similar, preferably the same effect on the amount of the metabolite as the gene or its entire coding sequence. This effect can be determined by well-known methods known in the art, for example involving the expression of the fragment in the organism or a biological test system derived from this organism (e.g. a cell culture or the like) and measuring the amount of the metabolite therein. This measurement may be compared with one obtained from a corresponding experiment undertaken with the gene or the entire coding sequence, and preferably with a measurement obtained from a control setting, wherein no heterologous nucleic acid molecule is expressed. If the amount of the metabolite upon fragment expression does not significantly deviate from that measured upon expression of the gene or the entire coding sequence, the fragment shows a similar or even the same function as the gene or the entire coding sequence.

The term “derivative of said coding sequence showing said function” refers to nucleotide sequences the complementary strand of which hybridizes with the coding sequence and wherein the derivative when expressed in a corresponding organism shows a similar, preferably the same effect on the amount of the metabolite with which the transcript of the coding sequence correlates as the gene or the coding sequence. This effect can be determined as described above in connection with fragments of the coding sequence.

If the coding sequence encodes a polypeptide, such a derivative may encode a polypeptide which has a homology, that is to say a sequence identity, of at least 30%, preferably of at least 40%, more preferably of at least 50%, even more preferably of at least 60% and particularly preferred of at least 70%, especially preferred of at least 80% and even more preferred of at least 90% to the entire amino acid sequence encoded by the coding sequence.

Moreover, such a derivative may have a homology, that is to say a sequence identity, of at least 40%, preferably of at least 50%, more preferably of at least 60%, even more preferably of more than 65%, in particular of at least 70%, especially preferred of at least 80%, in particular of at least 90% and evern more preferred of at least 95% when compared to the coding sequence.

The use of the present embodiment also relates to derivatives the sequence of which deviates from above-described hybridizing or homologous nucleotide sequences due to the degeneracy of the genetic code and which have a similar, preferably the same function as the coding sequence.

In the context of the present invention the term “hybridization” means hybridization under conventional hybridization conditions, preferably under stringent conditions, as for instance described in Sambrook and Russell (2001), Molecular Cloning: A Laboratory Manual, CSH Press, Cold Spring Harbor, N.Y., USA. In an especially preferred embodiment, the term “hybridization” means that hybridization occurs under the following conditions:

-   -   Hybridization buffer: 2×SSC; 10× Denhardt solution (Fikoll         400+PEG+BSA; ratio 1:1:1); 0.1% SDS; 5 mM EDTA; 50 mM Na2HPO4;     -    250 μg/ml of herring sperm DNA; 50 μg/ml of tRNA; or     -    0.25 M of sodium phosphate buffer, pH 7.2;     -    1 mM EDTA     -    7% SDS     -   Hybridization temperature T=60° C.     -   Washing buffer: 2×SSC; 0.1% SDS     -   Washing temperature T=60° C.

Derivatives which hybridize with the coding sequence of a gene the function of which is identified by applying the method of the invention can for instance be isolated from genomic libraries or cDNA libraries of bacteria, fungi, plants or animals. According to one aspect of the invention, it is preferred that such polynucleotides are from plant origin, particularly preferred from a plant belonging to the dicotyledons, more preferably from the family of Solanaceae. Preferably, the derivative is a variant, preferably an ortholog of said coding sequence. Alternatively, such derivatives can be prepared by genetic engineering or chemical synthesis.

Such hybridizing polynucleotides may be identified and isolated by using a nucleic acid molecule comprising the coding sequence or parts or reverse complements thereof, for instance by hybridization according to standard methods (see for instance Sambrook (2001). Fragments used as hybridization probes can also be synthetic fragments which are prepared by usual synthesis techniques, and the sequence of which is substantially identical with the coding sequence of the gene, a function of which has been determined by the method of the invention.

The molecules hybridizing with said coding sequence comprise fragments, derivatives and allelic variants of the specific coding sequence corresponding to the gene a function of which has been determined by applying the method of the invention.

Preferably, the degree of homology is determined by comparing the respective nucleotide sequence with the coding sequence of the gene a function of which has been identified by applying the method of the invention. When the sequences which are compared do not have the same length, the degree of homology preferably refers to the percentage of nucleotide residues in the shorter sequence which are identical to nucleotide residues in the longer sequence. The degree of homology can be determined conventionally using known computer programs such as the DNAstar program with the ClustalW analysis. This program can be obtained from DNASTAR, Inc., 1228 South Park Street, Madison, Wis. 53715 or from DNASTAR, Ltd., Abacus House, West Ealing, London W13 0AS UK (support@dnastar.com) and is accessible at the server of the EMBL outstation.

When using the Clustal analysis method to determine whether a particular sequence is, for instance, 80% identical to a reference sequence the settings are preferably as follows: Matrix: blosum 30; Open gap penalty: 10.0; Extend gap penalty: 0.05; Delay divergent: 40; Gap separation distance: 8 for comparisons of amino acid sequences. For nucleotide sequence comparisons, the Extend gap penalty is preferably set to 5.0.

Preferably, the degree of homology of the hybridizing polynucleotide is calculated over the complete length of its coding sequence. It is furthermore preferred that such a hybridizing polynucleotide, and in particular the coding sequence comprised therein, has a length of at least 300 nucleotides, preferably at least 500 nucleotides, more preferably of at least 750 nucleotides, even more preferably of at least 1000 mucleotides, particularly preferred of at least 1500 nucleotides and most preferably of at least 2000 nucleotides.

Preferably, sequences hybridizing to the coding sequence of the gene a function of which has been identified by applying the method of the invention comprise a region of homology of at least 90%, preferably of at least 93%, more preferably of at least 95%, still more preferably of at least 98% and particularly preferred of at least 99% identity to an above-described polynucleotide, wherein this region of homology has a length of at least 500 nucleotides, more preferably of at least 750 nucleotides, even more preferably of at least 1000 nucleotides, particularly preferred of at least 1500 nucleotides and most preferably of at least 2000 nucleotides.

Homology, moreover, means that there is a functional and/or structural equivalence between the corresponding polynucleotides or polypeptides encoded thereby. Polynucleotides which are homologous to the above-described molecules and represent derivatives of these molecules are normally variations of these molecules which represent modifications having the same biological function. They may be either naturally occurring variations, for instance sequences from other ecotypes, varieties, species, etc., or mutations, and said mutations may have formed naturally or may have been produced by deliberate mutagenesis. Furthermore, the variations may be synthetically produced sequences. The allelic variants may be naturally occurring variants or synthetically produced variants or variants produced by recombinant DNA techniques. Deviations from the above-described polynucleotides may have been produced, e.g., by deletion, substitution, insertion and/or recombination.

The polypeptides encoded by the different variants of the coding sequence of the gene, a function of which has been determined by applying the method of the invention, possess certain characteristics they have in common. These include for instance biological activity, molecular weight, immunological reactivity, conformation, etc., and physical properties, such as for instance the migration behavior in gel electrophoreses, chromatographic behavior, sedimentation coefficients, solubility, spectroscopic properties, stability, pH optimum, temperature optimum etc.

In connection with the present use of the invention, the term “polypeptide” refers to any polypeptide encoded by the above-mentioned gene, nucleic acid molecule, coding sequence, fragment or derivative. This polypeptide may, e.g., be a naturally purified product or a product of chemical synthetic procedures or produced by recombinant techniques from a prokaryotic or eukaryotic host (for example, by bacterial, yeast, higher plant, insect and mammalian cells in culture). Depending upon the host employed in a recombinant production procedure, the polypeptide may be glycosylated or non-glycosylated. The polypeptide may also include an initial methionine amino acid residue. It may be further modified to contain additional chemical moieties not normally part of the polypeptide. Those derivatized moieties may, e.g., improve the stability, solubility, the biological half life or absorption of the polypeptide. The moieties may also reduce or eliminate any undesirable side effects of the polypeptide and the like. An overview for these moieties can be found, e.g., in Remington's Pharmaceutical Sciences (18th ed., Mack Publishing Co., Easton, Pa. (1990)). Polyethylene glycol (PEG) is an example for such a chemical moiety which has been used for the preparation of therapeutic polypeptides. The attachment of PEG to polypeptides has been shown to protect them against proteolysis (Sada et al., J. Fermentation Bioengineering 71 (1991), 137-139). Various methods are available for the attachment of certain PEG moieties to polypeptides (for review see: Abuchowski et al., in “Enzymes as Drugs”; Holcerberg and Roberts, eds. (1981), 367-383). Generally, PEG molecules are connected to the polypeptide via a reactive group found on the polypeptide. Amino groups, e.g. on lysines or the amino terminus of the polypeptide are convenient for this attachment among others.

In addition, the present invention relates in a further embodiment to the use of a gene identified by the above-described method for identifying a gene which is capable of modifying the amount of a metabolite in an organism, of a nucleic acid molecule comprising the coding sequence of said gene or a fragment or derivative of said coding sequence which is capable of modifying the amount of a metabolite in an organism or of a polypeptide encoded by said gene or nucleic acid molecule for modifying the amount of a metabolite in an organism.

This use is in principle a preferred embodiment of the aforementioned use of a gene, the function of which has been determined by the method for determining the function of a gene, in that the “function” can be seen as the capacity of modifying the amount of a metabolite in an organism. Accordingly, the definitions for “coding sequence”, “nucleic acid molecule”, “fragment”, “derivative” and “polypeptide” given above likewise apply to the present embodiment.

Accordingly, also the preferred embodiments enumerated under (1) to (14), above, as to the uses of the genes corresponding to transcripts for applying the newly revealed functions also apply to the modification of the amount of the respective metabolite, preferably in a plant, especially in potato, more specifically in potato tuber.

Moreover, the present invention relates in a further embodiment to the use of a metabolite identified by the above-described method for identifying a metabolite which is capable of modifying the amount of a transcript in an organism for modifying the amount of a transcript in an organism.

This use is in principle a preferred embodiment of the above-outlined use of a gene, the function of which has been determined by the method for determining the function of a gene, in that the “function” can be seen as the capacity that the amount of the transcript of the gene can be modified by the metabolite.

Accordingly, the correlations enumerated under (1) to (14), above, give rise to preferred embodiments of the present use. In particular, it is conceivable that each of the metabolites mentioned there can be used for modifying the amount of the respective transcript for which the metabolite shows a correlation. These uses will preferably be applicable to plants, especially to potato, more specifically to potato tuber.

These and other embodiments are disclosed and encompassed by the description and examples of the present invention. Further literature concerning any one of the methods, uses and compounds to be employed in accordance with the present invention may be retrieved from public libraries, using for example electronic devices. For example the public database “Medline” may be utilized which is available on the Internet, for example under http://www.ncbi.nim.nih.gov/PubMed/medline.html. Further databases and addresses, such as http://www.ncbi.nlm.nih.gov/, http://www.infobiogen.fr/, http://www.fmi.ch/biology/research_tools.html, http://www.tigr.org/, are known to the person skilled in the art and can also be obtained using, e.g., http://www.google.de. An overview of patent information in biotechnology and a survey of relevant sources of patent information useful for retrospective searching and for current awareness is given in Berks, TIBTECH 12 (1994), 352-364.

Furthermore, the term “and/or” when occurring herein includes the meaning of “and”, “or” and “all or any other combination of the elements connected by said term”.

The present invention is further described by reference to the following non-limiting figures, tables and examples.

The Figures and the Tables show:

FIG. 1 is a visualization of the 1^(st) to 3^(rd) components from a principle component analysis (PCA) of gene expression profiles (a) and of metabolite profiles (b). The percentage of variance explained by each component is shown in parenthesis. The transgenic lines INV2-30 (INV) and SP 29 (SP), filled circles, and potato tuber after 8, 9, 10, 13 and 14 weeks growth, open circles.

FIG. 2 depicts correlations between metabolite and transcript levels of the analyzed systems. The correlation between the level of chemically defined metabolites and the level of each selected clone was assessed. All correlations with significant value P=0.01 when assessed by Spearman are presented on Table 3. Several representative examples are shown (all are plotted using the logarithmic scale, rs values are given in parenthesis): (a) sucrose transporter versus sucrose (rs=−0.52), (b) glutamate decarboxylase versus 4-aminobutyric acid (rs=0.55); (c) tryptophan synthase b chain 1 versus tryptophan; (rs=0.61) (d) tryptophan synthase b chain 1 versus tyrosine (rs=0.65); (e) ornithine carbamoyltransferase versus serine (rs=0.53); (f) ornithine carbamoyltransferase versus cysteine (rs=0.54); (g) aminotransferase-like protein, versus fructose-6-P (rs=0.85); (h) aminotransferase-like protein versus glucose-6-P (rs=0.85); (i) glutamate decarboxylase versus spermidine (rs=0.64); (j) glutamate decarboxylase versus tyrosine (rs=0.63); (k) CONSTANS-like protein versus ascorbate (rs=−0.72); (l) succinyl-CoA synthetase alpha subunit versus tocopherol (rs=−0.64); (m) transcription factor WRKY6 versus lysine (rs=0.51); (n) S-adenosyl-L-methionine synthetase versus lysine (rs=0.6); (o) ornithine carboxyltransferase versus lysine (rs=0.54); (p) caffeoyl-CoA O-methyltransferase versus lysine (rs=−0.52).

FIG. 3 displays the spotting scheme applied for the construction of the micro arrays used in the Examples 1 and 2.

The filter is organized in 16×24 block (FIG. 3A).

Description A1 to P24 corresponding to the position on the 384 well-plates.

The orientation is left-bottom since the origin of each plate A1 is located in the left bottom position of each block on the filter.

The description of R1-R24 and C1-C24 corresponding to the primary rows (R) and columns (C) in AIS program.

The secondary grit contain 4×4 spots (FIG. 3B). Each of the spots represent duplicates of the same clone (Figure C). In secondary grid 3 spots are left empty to quantify the local background.

The control DNA (human gene) is spotted at the position r4-c1.

Each secondary grid contains different clones from 6 different plates (T1-T6) (FIG. 3C).

The whole filter consists of 384 secondary grids which adds up to 2112 individual clones represented by the spots.

-   Table 1: Up and Down Regulated Transcripts in Developing Wild-Type     and in Transgenic Potato Tubers

For the: developing tubers the results from potato tuber after 8 weeks growth were chosen as the reference for calculating the relative amounts of transcripts in the subsequent stages of development. For the transgenic tubers, the results from wild-type tubers after 10 weeks growth were chosen as the reference.

a) 9 weeks

b) 10 weeks

c) 13 weeks

d) 14 weeks

e) SP29 line (SP)

f) INV30 line (INV2-30)

-   Table 2: Metabolite Levels in Potato Tubers

The data obtained from the transgenic lines are normalized to the mean response calculated for the wild-type tubes after 10 weeks of growing. For the developing wild-type tubers, 8 weeks grown tubers were used as reference. The values are presented as the mean ±SE of all independently determined replicates. Those metabolites that significantly differ from the reference are shown in boldface.

a) Developing wild-type tubers

b) Transgenic lines

-   Table 3: Significant Correlations Between Selected Transcripts and     Chemically Identified Metabolites

Correlations between selected transcripts (identified by reference to the EST clone to which it hybridises, see “EST ID” and “Annotation”) and metabolites (see “MB”) were calculated using the method of Spearman, taking correlations with significant value P=0.01 as the threshold of significance. Under “sig 0.001”, it is indicated whether a calculated correlation is also significant for p=0.001, the number 1 meaning significant and 0 non-significant. “NOP” stands for the number of correlated pairs.

-   Table 4: List of the EST Clones Spotted Onto the Microarray Used in     Examples 1 and 2     The following Examples illustrate the invention:

Experimental Set-Up 1. Plant Material

Solanum tubersosum L. cv Desiree was obtained from Saatzucht Lange AG (Bad Schwartau, Germany). The generation of the transgenic plant lines SP29 and INV2-30 used in this study has been detailed previously (Sonnewald, 1997; Tretheway, 2001; Roessner, 2001). Plants were handled as described in the literature (Tauberger, 2000; Regierer, 2002). Plants were maintained in tissue culture with a 16-hr.light/8-hr-dark regime on Murashige and Skoog (1962) medium that contained 2% sucrose. In the greenhouse, plants from all lines and wild-type were grown under the same light regime with a minimum of 250 μmol photons m⁻² sec⁻¹ at 22° C. Wild-type tubers were harvested after 8, 9 10, 13 and 14 weeks growing. Transgenic lines were harvested after 10 weeks of development.

2. Gene Expression Analysis 2.1 RNA Isolation

Total RNA was isolated from 2 g fresh weight of tuber tissue using REB isolation buffer (25 mM TrisHCl pH.8, 75 mM EDTA, 75 mM NaCl, 1% w/v SDS, 1 M β-MercaptoEtOH) and 10M LiCl2 as described by Logemann et al. (1987).

2.2 Microarray Construction

Microarrays were constructed on nylon filters as described previously (Thimm, 2001; Colebatch, 2002). More than 2000 tomato clones were collected from the cDNA library constructed in the laboratories of Dr. Steve Tanksley, Cornell. University Solanaceae Genome Network, Dr. Greg Martin, Boyce Thompson Institute and Dr. Jim Giovannoni, Boyce Thompson Institute and provided by TIGR—Institute for Genomic Research (Van der Hoeven, Plant Cell 14 (2002), 1441-1456). These ESTs correspond to approximately 1000 tomato genes which are highly homologous to those from potato (Fulton, 2002).

In particular, using the web site annotation http://www.tigr.org/tdb/tgi/lgi/ form LeGI Release 7.0—May 22, 2001, about one thousand interesting TCs (Tentative Consensus) were selected. For each TC, at least two ESTs were picked to the Solanum library, i.e. of each bacterial colony containing a specific EST, an alignot was selected and transferred to a new 96 well plate. (for the complete list of selected clones see Table 4). 96 additional potato clones were added, but the obtained results were not used for this work. The cDNA was amplified by PCR using LacZ-specific primers (forward LacZ1 5′ GCTTCCGGCT CGTATGTTGT GTG 3′ (SEQ ID NO:1) and reverse LacZ2 5′ AAAGGGGGATGTGCT GCAAGGCG 3′ (SEQ ID NO:2)) and Taq polymerase. The PCR products were selectively checked on an agarose gel before spotting. The PCR products were spotted automatically onto the nylon membranes (Biogrid, Biorobotics, Cambridge, UK; Nytran Supercharg, 22.2×22.2. cm, Schleicher and Schüll, Dassel, Germany). The Solanum library was spotted six times onto one membrane (for details of the spotting scheme see FIG. 3).

2.3 Reference Hybridization

To normalize the amount of spotted cDNA, a reference hybridization for each filter was carried but using a [³³P]-labeled PCR product-specific primer (T4 polynucleotide kinase, New England Biolabs, Beverly, Mass.; [³³P]ATP, Hartmann Analytic, Braunschweig, Germany; 5′ TTCCCAGTCACGA (SEQ ID NO:3)). The filters were hybridized at 5° C. overnight and washed for 40 min at 5° C. in Ssarc (4×SSC, 7% [v/v] Sarcosyl NL30, and 4 μM EDTA). Filters were exposed o/n on imaging plates and detected with phosphorimager (BAS-1800, Fuji, Tokyo). Radioactivity Was removed from the filters by washing two times in SSarc at 65° C. for 30 minutes. After every stripping, removing quality was checked by o/n exposition with imaging plates.

2.4 Reverse Transcriptase Labelling Reaction

For reverse transcription, 10 μg total RNA was used (SuperScript II, GibcoBRL, Karlsruhe, Germany; [³³P]CTP, Hartmann Analytic, Germany). After reverse transcription, RNA was hydrolyzed with NaOH (0.25N) and neutralized with HCl (0.2 N) and sodium phosphorylate buffer (40 mM, pH 7.2). Labelling efficiency was controlled by scintillation counting (LS6500, Beckman Munich) after removal of unincorporated oligonucleotides by Sephadex G-50 chromatography (NICK Columns, Amersham Pharmacia).

After pre-hybridisation for 2 h at 65° C. in Church buffer (7% [w/w] SDS, 1 mM EDTA, pH 8.0, and 0.5 M sodium phosphate, pH 7.2) containing salmon sperm DNA (100 ng ml⁻¹, Roth, Carl GmbH&Co, Karlsruhe, Germany), filters were hybridised with the labelled cDNA probe at 65° C. for 24 h. Washing steps were carried out at 65° C. for 20 min each with 1×SSC, 0.1% (w/v) SDS, 4 mM Na₂PO₄ (pH 1.2); 0.2×SSC, 0.1% (w/v) SDS, 4 mM Na₂PO₄ (pH 7.2); 0.1 SSC, 0.1% (w/v) SDS, 4 mM Na₂PO₄ (pH 7.2). The filters were exposed on imaging plates for 16 h and signals were detected using a phosphorimager (BAS-1800 II, Fuiji) followed by stripping for two times for 30 minutes at 80° C. (0.1% [w/v] SDS, 5 mM Na₂PO₄, pH 7.2). After every stripping, removing quality was checked by the o/n exposition with imaging plates. For transgenic lines and 10 weeks tubers, three repetitions of hybridisation with a newly synthesized and labelled cDNA probe of corresponding RNA were performed. For 8, 9, 13 and 14 weeks old tubers four repetitions were done.

2.5 Data Analysis

For data analysis, the signal intensities of the reference and complex hybridisation were quantified using the Array vision 5.1 software (Imaging Research Inc., Haverhill, UK). A predefined grid, determining the area of signal quantification, was manually optimised to ensure correct signal recording. The quantified signals, defined as photo-stimulated luminescence mm⁻², were assigned to the corresponding cDNA clones stored in a suitable database (“Haruspex”) (http://www.mpimp-golm.mpg.de/haruspex/index-e.html). The cDNAs on the filter were arranged as 4×4 arrays, each containing six doubly spotted clones, a human gene (desmin) (not used in this study), and an empty field to determine specific local background (LB) (for details see FIG. 3). In one membrane, the Solanum library was spotted six times (six block per membrane), and each block was analyzed separately. After each hybridization, six replicated results were obtained and normalized using the Haruspex database. From the available options, replacement by estimating values was used. Additionally, the normalized data was then subjected to Grubbs test (Grubbs 19.69 and Stefansky 1972) in order to detect outliers in the univariate data set.

For each clone, the average value for every repetition was calculated. Clones were described as differentially expressed in the tested situation while differences between average tested values and average reference values were two fold and additionally test showed significant change at the level of P 0.05.

3. Metabolite Analysis

The preparation and derivatisation of samples for metabolite analysis, and the subsequent operation of the GC-MS and evaluation of the resultant chromatograms and normalization of the results were carried out exactly as described (Roessner, 2001).

3.1 GC-TOF Analysis

For GC-TOF analysis, the organic phase was dried and dissolved in 50 μl of methoxamine hydrochloride (20 mg/mL pyridine) and incubated at 30° C. for 90 min with continuous shaking. Then 80 μL of N-Methyl-N-trimethylsilyltrifluoroacetamid (MSTFA) was added to derivatize polar functional groups at 37° C. for 30 min. The derivatized samples were stored at room temperature for 120 min before injection. GC-TOF analysis was performed on a HP 5890 gas chromatograph with standard liners and splitless injection at 230° C. injector temperature. The GC was operated at constant flow of 1 mL/min Helium and a 40 m 0.25 mm ID 0.25 μm RTX-5 column with 10 m integrated pre-column. The temperature gradient started at 80° C., was held isocratic for 2 min, and subsequently ramped at 15° C./min to a final temperature of 330° C. which was held for 6 min. 20 spectra per second were recorded between m/z 85 to 500. After data acquisition was finished, reference chromatograms were defined that had a maximum of detected peaks over a signal/noise threshold of 20 and used for automated peak identification based on mass spectral comparison to a standard NIST 98. Automated assignments of unique ions for each individual metabolite were taken as default as quantifiers, and manually corrected where necessary. All artifactual peaks caused by column bleeding or phtalates and polysiloxanes derived from MSTFA hydrolysation were removed from the results table. All data were normalized to plant mg FW and to the internal references and log-transformed. t-test, correlation analysis, and variance analysis were performed in Excel 5.

3.2 Two-Dimensional Liquid Chromatography/Mass Spectrometry.

The dried protein pellet was dissolved in freshly prepared 1M Urea in 0.05 M Tris buffer pH 7.6. The complex protein mixture was digested with modified trypsin (Böhringer Mannheim) according to the manufacturer's instructions. The tryptic digest was dried down and dissolved in 300 μwater (1% formic acid). Unsoluble material was removed by centrifugaton. An aliquot of the digest (˜100 μg protein) was injected onto two-dimensional chromatography on a thermofinnigan proteomeX system coupled to an LCQDecaXp ion trap (Thermofinnigan). The chromatographic separation was done according to manufacturer's instructions. After a 12 cycle run the MS/MS spectra were searched against an Arabidopsis thaliana database (downloaded from the TAIR homepage www.arabidopsis.org) using Turbosequest implemented in Bioworks 3.0 (Thermofinnigan). Matches were filtered according to Wolters et al. (2001). Additionally, we used the multiple scoring filter of Bioworks 3.0 with 50 percent ion coverage. For the quantification approach aliquots of the complex tryptic digest of Arabidopsis leaf protein (50 μL) were analysed on reversed phase chromatography. Quantification was achieved by integrating peak areas of target peptides representative for proteins. These peak areas were normalised to the sum of internal standard peptides that had been added to the mixture (Chelius et al. (2002), Bondarenko et al. (2002)).

4. Discriminant Analysis

Several different data transformations, distance measure and clustering methods were tested on the data set, before using principal component analysis (PCA). PCA was performed independently on the data sets obtained from transcript and metabolite profiling with the software package S-Plus 2000 (Insightfull, Berlin, Germany) using the default weighted covariance estimation function. The data was log10 transformed prior to further analysis and metabolites or ESTs that were not common to all samples were removed.

5. Correlation Analysis

Correlation analysis was used to select ESTs which gave highly reproducible results with respect to other ESTs of the consensus sequence from which they were derived. For this purpose the significance threshold was set to P>0.001. Only ESTs that were above this threshold according to the Spearman method and which appeared reliable during every experiment were selected for subsequent analysis. Table 1 shows the EST clones for which corresponding differentially expressed transcripts were observed. Correlations between selected transcripts and metabolites were calculated using the method of Spearman, taking correlations with significant value P=0.01.

EXAMPLE 1 Separate Profiling of Transcripts and Metabolites of Potato Tubers at Different Developmental Stages and of Transgenic Potato Tubers

The parallel analysis of a given biological system is described using two phenotyping technologies, the current technology of metabolic profiling based on GC-MS analysis and gene expression analysis using classical array technology. In attempting these experiments, it was first tried to answer the question what the relative power of the two phenotyping technologies is to discriminate biological systems which either differ in the developmental state or exhibit well characterized transgenic changes.

When these experiments were designed, it was decided to use a plant system, namely the potato tuber system, to evaluate the above questions. The reasons for this were two-fold: first, the potato tuber displays well-defined but nevertheless highly related developmental stages and allows the assessment of a number of well-characterized transgenic situations. Second, the laboratory of the inventors is very well acquainted with the analysis of the potato tubers on both the biochemical and the molecular levels (Fernie, 2002). As a first step, the expression of 1000 genes represented by at least two expressed sequence tags (ESTs) comprising the genes of many transcription factors and a wide variety of biosynthetic genes were analysed on a custom array. After analysing the data sets obtained, 279 ESTs were selected which gave highly reproducible results with respect to the consensus sequence from which they were derived. In order to see whether various developmental stages could be discriminated from one another and from the transcript profiles of transgenic potato tubers ectopically expressing a more efficient pathway of sucrose mobilization (Roessner, 2001), a principal component analysis (PCA) was performed. Table 1 is a presentation of those clones of which the corresponding transcripts are differentially expressed. As can be seen in FIG. 1 a, some of the developmental stages can be well distinguished from each other on the basis of their transcript profiles. In this respect, the clear differentiation of tubers harvested after 10 weeks of growth from the other developmental stages is most notable, a fact which may be attributed to the high metabolic activity at this developmental stage. However, it was also observed that the transcript levels of the transgenic tubers could not be discriminated either from each other nor from the corresponding wild-type tuber which was quite surprising. It is important to note that a similar picture was observed following principal component analysis of the entire transcript data set (data not shown). Whilst it is clear that the tuber samples harvested following ten weeks of plant growth were strikingly different from those harvested at other developmental stages, the fact remains that these results suggest that the transcriptional variation during development is greater than that following a relatively severe genetic perturbation of the primary metabolism (Roessner, 2001).

Metabolic profiling was then carried out on samples corresponding to those in the above-described transcript analysis in order to determine the levels of the major metabolites of primary metabolism including sugars, sugar alcohols, organic acids, amino acids as well as the nutritionally important compounds ascorbate and tocopherol. The corresponding metabolite profiles are depicted in Table 2. When a principal component analysis was carried out on the data set obtained from the metabolic profiling studies (FIG. 1 b), a picture was observed different from that seen upon analysis of the transcript data. In this instance, the transgenic plants clustered completely independently (both with respect to the wild-type control and to one another). With regard to the different developmental stages of the wild-type plants, however, the metabolite complement samples taken after 10 weeks of growth were relatively similar to those taken at other time points.

In conclusion, the discriminatory power of transcript and metabolite profiling approaches are different with metabolite profiling allowing a greater resolution of the different systems studied here. Whether or not this reflects the fact that changes on the transcript level are less pronounced as compared to changes on the metabolite level or merely highlights limitations of the profiling technologies used remains an open question. However, whatever the reason, these results imply that the discrimination of biological systems should be performed at more than one level.

EXAMPLE 2 Parallel Transcript and Metabolite Profiling of Potato Tubers and Correlation Analysis of the Two Data Sets Obtained

As a further question, it was examined whether the combined analysis of transcript and metabolite profiling data presents a useful approach for the identification of candidate genes that may change the metabolic composition of a given biological system. For this purpose, all the transcript and metabolite data points obtained in the analysis described in Example 1 were run through pairwise correlation analysis in order to determine for each transcript whether it is correlated with any of the metabolites. Out of the 23715 analysed pairs 329 positive and 189 negative correlation's were identified. The used significance threshold of P=0.01 in the non-parametric Spearman's rank correlation analysis is a rather conservative estimation of the number of chance correlations. Therefore, the identification of 518 correlations of high statistical significance was a surprising result. A couple of representative correlations is shown in FIG. 2 and discussed in detail below, whilst the entire list is given in Table 3.

First, as with any new approach it is important to see whether the data obtained is in agreement with observations made following different, more established experimental strategies. This is clearly the case if one contemplates for instance the strong negative correlation between sucrose and sucrose transporter expression (FIG. 2 a) and the strong positive correlation between 4-aminobutyric acid and glutamate decarboxylase isoform I (FIG. 2 b). Both correlations have previously been reported in the literature (Vaughn, 2002; Facchini, 2000), thus providing a confirmation of the validity of the herein presented new approach. Second, many further correlations seem to have a functional basis that can be explained retrospectively. The positive correlations of both tryptophan and tyrosine with the β2chain of tryptophan synthase (FIGS. 2 c, 2 d) and ornithine carbamoyltransferase with serine and cysteine (FIGS. 2 e, 2 f) are two such examples. Third, although several of the correlations, such as those described above, were predictable, the majority of the correlations obtained was novel and unpredictable since they are not directly related to the biochemical pathway in which the respective gene products participate. Several correlations were identified between transcripts and metabolites of the same or related pathways a fact that may strengthen the interpretation of these linkages. Examples of such instances include aminotransferase which correlates with both fructose-6-phosphate and glucose-6-phosphate (FIGS. 2 g, 2 h). These two correlations could not be predicted on the basis of the previous knowledge. But the existence of one of these correlations makes it likely that also the other one exists, as it has been shown in the present studies. These findings may offer hints to the function of the genes involved (the elucidation of which, if carried out by conventional methods, requires a huge amount of research effort). It is also interesting to note that several transcripts correlate with more than one metabolite, such as the aminotransferase mentioned above. Other examples include glutamate decarboxylase isoform I which correlates both with spermidine (FIG. 2 i) and tyrosine (FIG. 2 j) and various transcription factors correlating with sucrose, 4-aminobutyric acid and tryptophan. Finally it is exciting to see that nutritionally important metabolites such as ascorbate, tocopherol and lysine were tightly correlated with the expression levels of various enzymes or transcription factors: e.g. ascorbate being negatively correlated, with a homologue of the clock gene CONSTANS (FIG. 2 k), tocopherol being negatively correlated with succinyl CoA synthetase (FIG. 2 l) and lysine being positively correlated with the transcription factor WRKY6 (FIG. 2 m), S-adenosyl-L-methionine synthetase (FIG. 2 n) and ornithine carbamoyltransferase (FIG. 2 o) and negatively correlated with caffeoyl-CoA O-methyltransferase (FIG. 2 p). It is believed that these essentially unexpected correlations are of great potential for biotechnological applications in which it is the goal to modify the metabolite composition by genetic means. The approach of linking transcript and metabolite data via pair-wise correlation analysis presents a very powerful tool for the rapid identification of candidate genes, which then have to be tested for their value as regards applicability via further experimentation.

As a conclusion from the afore-described experiments, one has to note that, although, as might have been expected from previous experimental work aimed at comparing the transcript and protein levels (Ideker, 2001: Gygi, 1999; Futcher, 1999) and mathematical studies (TerKuile, 2001), the number of strong, metabolite-transcript correlations observed is relatively small, it is conceivable that they allow the generation of clearly verifiable hypotheses. Of particular interest in this regard are the observation of the correlation of genes with the essential amino acid lysine and with the vitamins ascorbate and tocopherol. These linkages define strong candidate genes for the manipulation of the content of these nutritionally important compounds in plants.

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TABLE 1 ANNOTATION EST ID XFOLD (a) List of up and down regulated clones in 9 weeks old potato tuber S-adenosyl-L-methionine synthetase CTOF3K21 0.20 glycogen (starch) synthase precursor {Solanum CTOF21A12 0.22 tuberosum}SP|Q00775|UGST_SOLTU GRANULE-BOUND GLYCOGEN Similar to gb|AF135422 GDP-mannose pyrophosphorylase A (GMPPA) from CLET27N17 0.27 Homo sapiens. ESTs gb|AA712990, NADH-ubiquinone oxidoreductase 20 kDa subunit precursor {Solanum CLEG33O5 0.33 tuberosum}SP|Q43844|NUKM_SOLTU NAD S-adenosylmethionine:2-demethylmenaquinone methyltransferase-like protein CLED30J21 0.38 {Arabidopsis thaliana} NADH-ubiquinone oxidoreductase 20 kDa subunit precursor {Solanum CLED16D1 0.40 tuberosum}SP|Q43844|NUKM_SOLTU NAD transcription factor CRC {Arabidopsis CLED15E7 0.46 thaliana}GP|12325076|gb|AAG52485.1|AC018364_3|AC018364 transc S-adenosylmethionine:2-demethylmenaquinone methyltransferase-like protein CTOF26K3 0.48 {Arabidopsis thaliana} transcription factor IIA small subunit {Arabidopsis CTOE6J10 0.49 thaliana}GP|5051786|emb|CAB45079.1||AL078637 tr cytochrome P450, putative {Arabidopsis thaliana}PIR|F86441|F86441 probable CTOF3J9 0.49 cytochrome P450 [importe hydroxycinnamoyl-CoA:tyramine N-(hydroxycinnamoyl)transferase {Capsicum CLEC4A12 0.50 annuum} putative C3HC4-type RING zinc finger protein {Arabidopsis CLEC32P10 2.00 thaliana}PIR|B84813|B84813 probable RING bHLH transcription factor GBOF-1 {Tulipa gesneriana} CLEM17A5 3.68 (b) List of up and down regulated clones in 10 weeks old potato tuber caffeoyl-CoA O-methyltransferase 5 {Nicotiana CLEZ20I22 0.44 tabacum}GP|1679853|emb|CAB05369.1||Z82982 caffeoyl-Co “putative ABC transporter; 60211-54925 {Arabidopsis thaliana}PIR|E96742|E96742 CLED21K4 0.45 probable ABC transpor” aldose 1-epimerase-like protein {Arabidopsis thaliana} CLEZ10I24 0.46 NADH-dependent glutamate synthase {Arabidopsis thaliana} CLEC38H15 0.47 glutamine synthetase I {Medicago truncatula} CLEC16M12 0.48 URIDYLATE KINASE (EC 2.7.4.—) (UK) (URIDINE MONOPHOSPHATE KINASE) CLEY26B11 2.00 (UMP KINASE) (UMP/CMP KINASE).GP| putative cytochrome P450 {Solanum chacoense}SP|P93530|C7D6_SOLCH CLED28H13 2.02 CYTOCHROME P450 71D6 (EC 1.14.—.—) zinc finger protein-like {Arabidopsis thaliana} CLEG37C14 2.06 NADH-ubiquinone oxidoreductase 20 kDa subunit precursor {Solanum CLEG33O5 2.09 tuberosum}SP|Q43844|NUKM_SOLTU NAD tyramine hydroxycinnamoyltransferase {Nicotiana tabacum} CLEZ9E23 2.10 zinc finger protein-like {Arabidopsis thaliana} CTOF19M22 2.11 putative homeodomain transcription factor {Arabidopsis CLED30M20 2.11 thaliana}PIR|H84774|H84774 probable homeodom sugar transporter like protein {Arabidopsis CLPP11N17 2.16 thaliana}GP|2464913|emb|CAB16808.1||Z99708 sugar transp transcription factor CRC {Arabidopsis CLED4O9 2.21 thaliana}GP|12325076|gb|AAG52485.1|AC018364_3|AC018384 transc putative cytochrome P450 {Solanum chacoense}SP|P93530|C7D6_SOLCH CLED4O17 2.27 CYTOCHROME P450 71D6 (EC 1.14.—.—) ALTERNATIVE OXIDASE 1 PRECURSOR (EC 1.—.—.—). CLEY14I23 2.30 GP|558054|gb|AAC60576.1||S71335 alternative oxidase, A UDP-glucose:salicylic acid glucosyltransferase {Nicotiana tabacum} CLED25E6 2.31 ALTERNATIVE OXIDASE 1 PRECURSOR (EC 1.—.—.—). CLEY7C9 2.33 GP|558054|gb|AAC60576.1||S71335 alternative oxidase, A lysine-ketoglutarate reductase/saccharopine dehydrogenase bifunctional enzyme CLEC6K9 2.34 {Arabidopsis thaliana} sugar-phosphate isomerase-like protein {Arabidopsis thaliana}PIR|T47628|T47628 CLEY19P11 2.35 sugar-phosphate isom S-adenosylmethionine:2-demethylmenaquinone methyltransferase-like protein CTOF26K3 2.37 {Arabidopsis thaliana} “ornithine carbamoyltransferase; OCTase {Canavalia CLED6P9 2.38 lineata}GP|12003188|gb|AAG43481.1|AF203688_1|AF20” transcription factor TEIL {Nicotiana tabacum} CLEG39L11 2.38 transcription factor WRKY6 {Arabidopsis CLEI5A6 2.38 thaliana}GP|12658412|gb|AAK01128.1|AF331713_1|AF331713 tran PROBABLE VACUOLAR ATP SYNTHASE SUBUNIT F (EC 3.6.1.34)(V-ATPASE CLEX11L22 2.38 F SUBUNIT) (VACUOLAR PROTON PUMP F ATP synthase delta′ subunit, mitochondrial precursor {Ipomoea CTOF10I1 2.39 batatas}SP|Q40089|ATP4_IPOBA ATP SYNT putative homeodomain transcription factor {Arabidopsis CLED21A22 2.40 thaliana}PIR|F84565|F84565 probable homeodom contains similarity to sugar transporters ({grave over (P)}fam: sugaŕ_tr.hmm, score: 395.91) CTOD2G24 2.41 {Arabidopsis thaliana} cytochrome P450-like protein {Arabidopsis CLHT23L11 2.41 thaliana}GP|7270932|emb|CAB80611.1||AL161595 cytochrome P succinate dehydrogenase flavoprotein alpha subunit {Arabidopsis CLEZ9G24 2.42 thaliana}GP|8843734|dbj|BAA97282.1| cytochrome p450 lxxia4 {Solanum melongena}SP|P37117|C714_SOLME CLED11B9 2.43 CYTOCHROME P450 71A4 (EC 1.14.—.—) ( glycerol-3-phosphate dehydrogenase {Arabidopsis thaliana}PIR|F84832|F84832 CLES5M24 2.44 glycerol-3-phosphate deh putative monosaccharide transporter 1 {Petunia x hybrida} CLPP11G6 2.45 sugar transporter like protein {Arabidopsis CLPP7D3 2.46 thaliana}GP|2464913|emb|CAB16808.1||Z99708 sugar transp CCAAT box binding factor/transcription factor Hap2a {Arabidopsis CLEG43E15 2.46 thaliana}PIR|T49898|T49898 CCAAT fructokinase 1 {Arabidopsis CLPP13M11 2.51 thaliana}GP|13878053|gb|AAK44104.1|AF370289_1|AF370289 putative fructok 4-hydroxyphenylpyruvate dioxygenase {Solenostemon scutellarioides} CLEC33J10 2.54 delta 1-pyrroline-5-carboxylate synthetase CTOE2C17 2.54 URIDYLATE KINASE (EC 2.7.4.—) (UK) (URIDINE MONOPHOSPHATE KINASE) CLEM3K4 2.56 (UMP KINASE) (UMP/CMP KINASE).GP| transcription factor WRKY6 {Arabidopsis CLEC11I13 2.58 thaliana}GP|12658412|gb|AAK01128.1|AF331713_1|AF331713 tran contains similarity to sugar transporters (Pfam: sugar_tr.hmm, score: 395.91) CLPP7N18 2.59 {Arabidopsis thaliana} Dof zinc finger protein {Arabidopsis CLED28N11 2.59 thaliana}GP|9280230|dbj|BAB01720.1||AB023045 Dof zin{umlaut over (c)} finger p bHLH transcription factor GBOF-1 {Tulipa gesneriana} CLED22C14 2.60 acetylornithine aminotransferase precursor {Alnus CLED24N6 2.62 glutinosa}SP|O04866|ARGD_ALNGL ACETYLORNITHINE AM glucosyl transferase {Nicotiana tabacum}GP|1805359|dbj|BAA19155.1||AB000623 CLEG32P19 2.62 glucosyl transferase {N glutamate decarboxylase isozyme 1 {Nicotiana tabacum} CLPP9O23 2.63 putative cytochrome P450 CLES20P12 2.63 glutamate decarboxylase isozyme 1 {Nicotiana tabacum} CLPP5L24 2.67 TRYPTOPHAN SYNTHASE BETA CHAIN 2 PRECURSOR (EC CLEI13J17 2.69 4.2.1.20).GP|2792520|gb|AAB97087.1||AF042320 tryptop MADS-box transcription factor FBP21 {Petunia x hybrida} CLEX2O20 2.75 cytochrome P450 like_TBP {Nicotiana CTOF7K11 2.75 tabacum}GP|1545805|dbj|BAA10929.1||D64052 cytochrome P450 like_(—) homeodomain protein CLED11B1 2.78 TRYPTOPHAN SYNTHASE BETA CHAIN 2 PRECURSOR (EC CLEM4L3 2.79 4.2.1.20).GP|2792520|gb|AAB97087.1||AF042320 tryptop ethylene-responsive transcriptional coactivator CTOF23I9 2.80 NADH-ubiquinone oxidoreductase 20 kDa subunit precursor {Solanum CLED16D1 2.85 tuberosum}SP|Q43844|NUKM_SOLTU NAD ALTERNATIVE OXIDASE 1 PRECURSOR (EC 1.—.—.—). CLPP2C18 2.86 GP|558054|gb|AAC60576.1||S71335 alternative oxidase, A alanine aminotransferase {Arabidopsis thaliana} CLEC29A19 2.92 glucosyltransferase-like protein {Arabidopsis thaliana} CLEC6D16 2.93 hydroxycinnamoyl-CoA:tyramine N-(hydroxycinnamoyl)transferase {Capsicum CLEC36G5 2.97 annuum} SNAP25A protein {Arabidopsis thaliana}GP|5731763|emb|CAB52582.1||X92419 CLET10A17 2.97 SNAP25A protein {Arabidopsi phosphate/phosphoenolpyruvate translocator-like protein {Arabidopsis thaliana} CLPP8K20 3.13 ADP-glucose pyrophosphorylase small subunit CLEM19M11 3.18 homeodomain protein CTOF6M4 3.22 ATP synthase delta′ subunit, mitochondrial precursor {Ipomoea CLEY15P13 3.26 batatas}SP|Q40089|ATP4_IPOBA ATP SYNT ethylene-responsive transcriptional coactivator CLEC40C16 3.31 putative homeodomain transcription factor {Arabidopsis CLED15E8 3.33 thaliana}PIR|H84774|H84774 probable homeodom dTDP-glucose 4-6-dehydratases-like protein {Arabidopsis CLEZ16P14 3.33 thaliana}PIR|T45701|T45701 dTDP-glucose 4-6 “putative transcription factor BTF3 (RNA polymerase B transcription factor 3); CLEZ8J8 3.33 26343-27201 {Arabidops” Similar to acyl carrier protein, mitochondrial precursor (ACP) NADH-ubiquinone CLEZ20E22 3.37 oxidoreductase 9.6 KD putative C3HC4-type RING zinc finger protein {Arabidopsis CLEC32P10 3.45 thaliana}PIR|B84813|B84813 probable RING “putative transcription factor BTF3 (RNA polymerase B transcription factor 3); CTOF23N20 3.50 26343-27201 {Arabidops” flavanone 3-hydroxylase-like protein {Arabidopsis thaliana} CTOE12M9 3.55 glucosyltransferase-like protein {Arabidopsis thaliana} CLED34H6 3.58 MADS-box transcription factor FBP21 {Petunia x hybrida} CLET8H21 3.59 phosphate/phosphoenolpyruvate translocator protein-like {Arabidopsis thaliana} CLEG41L23 3.61 putative homeodomain transcription factor {Arabidopsis CLEG35I11 3.65 thaliana}PIR|F84565|F84565 probable homeodom putative C3HC4-type RING zinc finger protein {Arabidopsis CLEX12A9 3.72 thaliana}PIR|B84813|B84813 probable RING NADH-cytochrome b5 reductase {Arabidopsis CLEY21D5 3.73 thaliana}GP|4240118|dbj|BAA74838.1||AB007800 NADH-cytochr mas-binding factor MBF2 = transcription factor TGA1a homolog {Solanum CLEY24E3 3.74 tuberosum = potatoes, root, Peptid SNAP25A protein {Arabidopsis thaliana}GP|5731763|emb|CAB52582.1||X92419 CLEM23I12 3.76 SNAP25A protein {Arabidopsi serine/threonine-specific protein kinase NAK {Arabidopsis CLER2B1 3.82 thaliana}PIR|T48250|T48250 serine/threoni dehydroquinate dehydratase/shikimate:NADP oxidoreductase CLEG39N19 3.86 S-adenosylmethionine:2-demethylmenaquinone methyltransferase-like protein CLED30J21 3.87 {Arabidopsis thaliana} putative NADH-ubiquinone oxireductase {Arabidopsis CLEG27G1 3.90 thaliana}PIR|C84588|C84588 probable NADH-ubiquin S-adenosyl-L-methionine synthetase CTOF10L8 3.97 fructose-6-phosphate 2-kinase/fructose-2,6-bisphosphatase {Solanum CLEI12O14 4.04 tuberosum}PIR|T07016|T07016 6-ph fructose-6-phosphate 2-kinase/fructose-2,6-bisphosphatase {Solanum CLEI15M10 4.07 tuberosum}PIR|T07016|T07016 6-ph Putative UDP-glucose glucosyltransferase {Arabidopsis CLEX11K13 4.10 thaliana}PIR|H86356|H86356 probable UDP-gluco phosphate/phosphoenolpyruvate translocator-like protein {Arabidopsis thaliana} CLPP9C20 4.31 w-3 desaturase (Solanum tuberosum}PIR|T07685|T07685 omega-3 fatty acid CLEG33A5 4.49 desaturase (EC 1.14.99.—)- glycogen (starch) synthase precursor {Solanum CTOF21A12 4.60 tuberosum}SP|Q00775|UGST_SOLTU GRANULE-BOUND GLYCOGEN glycogen (starch) synthase precursor {Solanum CLPT10L12 4.68 tuberosum}SP|Q00775|UGST_SOLTU GRANULE-BOUND GLYCOGEN acetylornithine aminotransferase precursor {Alnus CLEI11O22 4.70 glutinosa}SP|O04866|ARGD_ALNGL ACETYLORNITHINE AM CCAAT box binding factor/transcription factor Hap2a {Arabidopsis CLEC15K2 4.79 thaliana}PIR|T49898|T49898 CCAAT HD-Zip protein [Arabidopsis thaliana] CLEC13O19 4.84 UDP-glucose dehydrogenase-like protein {Arabidopsis CLEY2E3 4.88 thaliana}PIR|T51527|T51527 UDP-glucose dehydrog ALTERNATIVE OXIDASE 1 PRECURSOR (EC 1.—.—.—). CLEY14E21 4.90 GP|558054|gb|AAC60576.1||S71335 alternative oxidase, A MYB-like DNA-binding protein {Catharanthus roseus} CTOF22G14 4.93 similar to ATPases associated with various cellular activites (Pfam: AAA.hmm, CLEG8L3 4.96 score: 230.91) {Arabid putative cytochrome P450 CTOE2F5 5.01 cytochrome P450 like_TBP {Nicotiana CLPP10E22 5.07 tabacum}GP|1545805|dbj|BAA10929.1||D64052 cytochrome P450 like_(—) osmotic stress-induced zinc-finger protein {Nicotiana tabacum}PIR|T01985|T01985 CLEX4M2 5.07 zinc-finger protein phosphate/phosphoenolpyruvate translocator protein-like {Arabidopsis thaliana} CLEG30O13 5.60 TOM (target of myb1)-like protein {Arabidopsis thaliana}PIR|T51543|T51543 TOM CLHT6E15 5.73 (target of myb1)-like osmotic stress-induced zinc-finger protein {Nicotiana tabacum}PIR|T01985|T01985 CLEC21H24 5.89 zinc-finger protein TOM (target of myb1)-like protein {Arabidopsis thaliana}PIR|T51543|T51543 TOM CLHT18D23 6.01 (target of myb1)-like similar to ATPases associated with various cellular activites (Pfam: AAA.hmm, CLEG12O3 6.47 score: 230.91) {Arabid “putative ABC transporter; 73228-76244 {Arabidopsis thaliana}” CLEN21M4 6.57 ADP-glucose pyrophosphorylase small subunit CLES16N17 6.94 bHLH transcription factor GBOF-1 {Tulipa gesneriana} CLEM17A5 7.00 cytochrome P450-like protein {Arabidopsis CLEG12G7 7.29 thaliana}GP|7270932|emb|CAB80611.1||AL161595 cytochrome P 76 kDa mitochondrial complex I subunit {Solanum CLEG28D24 7.32 tuberosum}SP|Q43644|NUAM_SOLTU NADH-UBIQUINONE OXID dehydroquinate dehydratase/shikimate:NADP oxidoreductase CLEM21P8 10.01 76 kDa mitochondrial complex I subunit {Solanum CLET38C16-1 10.16 tuberosum}SP|Q43644|NUAM_SOLTU NADH-UBIQUINONE OXID (c) List of up and down regulated clones in 13 weeks old potato tuber cytochrome P450 like_TBP {Nicotiana CTOF7K11 0.16 tabacum}GP|1545805|dbj|BAA10929.1||D64052 cytochrome P450 like_(—) S-adenosyl-L-methionine synthetase CTOF3K21 0.18 Similar to gb|AF135422 GDP-mannose pyrophosphorylase A (GMPPA) from Homo CLET27N17 0.25 sapiens. ESTs gb|AA712990, glycogen (starch) synthase precursor {Solanum CTOF21A12 0.28 tuberosum}SP|Q00775|UGST_SOLTU GRANULE-BOUND GLYCOGEN NADH-ubiquinone oxidoreductase 20 kDa subunit precursor {Solanum CLEG33O5 0.30 tuberosum}SP|Q43844|NUKM_SOLTU NAD PROBABLE VACUOLAR ATP SYNTHASE SUBUNIT F (EC 3.6.1.34) (V-ATPASE CLEX11L22 0.36 F SUBUNIT) (VACUOLAR PROTON PUMP F Similar to acyl carrier protein, mitochondrial precursor (ACP) NADH-ubiquinone CLED7G23 0.45 oxidoreductase 9.6 KD fructose-6-phosphate 2-kinase/fructose-2,6-bisphosphatase {Solanum CLEI12O14 0.46 tuberosum}PIR|T07016|T07016 6-ph Dof zinc finger protein {Arabidopsis CLED28N11 0.48 thaliana}GP|9280230|dbj|BAB01720.1||AB023045 Dof zinc finger p chorismate synthase 1 precursor 3-phosphate phospholyase 1) {Lycopersicon CTOF26D9 0.49 esculentum}SP|Q42884|ARC1 UDP-glucose:salicylic acid glucosyltransferase {Nicotiana tabacum} CLEG1L22 2.04 NADH-cytochrome b5 reductase {Arabidopsis CLEY21D5 2.04 thaliana}GP|4240118|dbj|BAA74838.1||AB007800 NADH-cytochr putative C3HC4-type RING zinc finger protein {Arabidopsis CLEC32P10 2.25 thaliana}PIR|B84813|B84813 probable RING bHLH transcription factor GBOF-1 {Tulipa gesneriana} CLEM17A5 2.54 (d) List of up and down regulated clones in 14 weeks old potato tuber. transcription factor WRKY6 {Arabidopsis CLEI5A6 0.22 thaliana}GP|12658412|gb|AAK01128.1|AF331713_1|AF331713 tran transcription factor IIA small subunit {Arabidopsis CTOE6J10 0.42 thaliana}GP|5051786|emb|CAB45079.1||AL078637 tr dTDP-glucose 4-6-dehydratases-like protein {Arabidopsis CLEZ16P14 0.45 thaliana}PIR|T45701|T45701 dTDP-glucose 4-6 Zn finger protein {Nicotiana tabacum}GP|1360078|emb|CAA66601.1||X97942 Zn CLED15J6 0.46 finger protein {Nicotiana hydroxycinnamoyl-CoA:tyramine N-(hydroxycinnamoyl)transferase {Capsicum CLEC4A12 0.46 annuum} “ornithine carbamoyltransferase; OCTase {Canavalia CLED6P9 0.46 lineata}GP|12003188|gb|AAG43481.1|AF203688_1|AF20” alpha-glucosidase {Solanum tuberosum subsp. tuberosum} CLED6K9 0.47 alanine aminotransferase {Arabidopsis thaliana} CLEG9A20 0.48 bHLH transcription factor GBOF-1 {Tulipa gesneriana} CLEM17A5 2.69 cytochrome P450 like_TBP {Nicotiana CLPP10E22 3.41 tabacum}GP|1545805|dbj|BAA10929.1||D64052 cytochrome P450 like_(—) (e) List of up and down regulated clones in transgenic tubers - line SP29 ADP-glucose pyrophosphorylase small subunit CLES16N17 0.49 UDP-glucose:salicylic acid glucosyltransferase {Nicotiana tabacum} CLEG1L22 2.13 (f) List of up and down regulated clones in transgenic tubers - line INV30 S-adenosyl-L-methionine synthetase CTOF3K21 0.42 Dof zinc finger protein {Arabidopsis CLED28N11 0.49 thaliana}GP|9280230|dbj|BAB01720.1||AB023045 Dof zinc finger p putative cytochrome P450 CTOE2F5 0.49 cytochrome P450 {Arabidopsis thaliana} CLEI13B24 2.16 transcription factor TEIL {Nicotiana tabacum} CLEG42L9 2.20 “putative ABC transporter; 73228-76244 {Arabidopsis thaliana}” CLEG42N24 2.38 UDP-glucose:salicylic acid glucosyltransferase {Nicotiana tabacum} CLEG1L22 3.02 Putative UDP-glucose glucosyltransferase {Arabidopsis CLEX13P4 3.08 thaliana}PIR|H86356|H86356 probable UDP-gluco

TABLE 2 (a) Potato tuber development Metabolite 9 weeks SE 10 weeks SE 13 weeks SE 14 weeks SE 8 weeks SE 5-oxoproline 0.43 ±0.21 0.72 ±0.18 0.43 ±0.37 0.74 ±0.72 1.00 ±0.28 aconitate 1.68 ±0.09 0.78 ±0.07 0.98 ±0.20 1.12 ±0.27 1.00 ±0.23 alanine 0.58 ±0.16 0.91 ±0.35 0.24 ±0.31 0.27 ±0.53 1.00 ±0.20 arginine 0.87 ±0.25 0.69 ±0.19 0.69 ±0.07 1.19 ±0.42 1.00 ±0.10 asparagine 1.24 ±0.29 1.02 ±0.37 1.79 ±0.37 2.43 ±0.42 1.00 ±0.12 aspartate 0.94 ±0.08 0.66 ±0.12 0.86 ±0.08 0.76 ±0.04 1.00 ±0.08 α-tocopherol 0.75 ±0.07 0.35 ±0.07 0.41 ±0.08 0.80 ±0.90 1.00 ±0.24 β-alanine 3.28 ±0.17 2.37 ±0.52 1.23 ±0.12 1.65 ±0.50 1.00 ±0.43 γ-caffeate 1.62 ±0.23 0.70 ±0.27 0.56 ±0.14 0.48 ±0.20 1.00 ±0.05 citramalate 1.69 ±0.09 0.63 ±0.16 1.11 ±0.14 0.80 ±0.26 1.00 ±0.14 citrate 1.29 ±0.09 0.80 ±0.06 0.93 ±0.11 0.90 ±0.06 1.00 ±0.05 cysteine 0.89 ±0.05 0.73 ±0.10 0.74 ±0.09 0.59 ±0.21 1.00 ±0.10 dehydroascorbate 0.37 ±0.51 0.37 ±0.16 1.12 ±0.36 0.36 ±0.49 1.00 ±0.68 D-isoascorbate 0.67 ±0.22 0.91 ±0.23 0.94 ±0.25 0.97 ±0.41 1.00 ±0.13 erythritol 0.90 ±0.20 0.64 ±0.18 0.94 ±0.27 0.98 ±0.35 1.00 ±0.20 FA 16:0 0.92 ±0.12 0.61 ±0.12 0.89 ±0.08 0.84 ±0.07 1.00 ±0.06 FA 18:0 0.96 ±0.12 0.62 ±0.19 0.99 ±0.08 0.91 ±0.08 1.00 ±0.07 FA 9,12(Z,Z)- 0.91 ±0.10 0.73 ±0.13 0.74 ±0.07 0.64 ±0.10 1.00 ±0.07 18:2 fructose-6-P 0.70 ±0.16 0.50 ±0.06 0.59 ±0.06 0.74 ±0.32 1.00 ±0.36 fructose 0.24 ±0.06 0.10 ±0.24 0.10 ±0.16 0.10 ±0.33 1.00 ±0.46 fucose 0.73 ±0.17 0.48 ±0.17 0.69 ±0.17 0.83 ±0.56 1.00 ±0.21 fumarate 0.45 ±0.13 0.24 ±0.08 0.24 ±0.33 0.20 ±0.60 1.00 ±0.58 GABA 1.34 ±0.06 1.48 ±0.07 1.39 ±0.12 1.51 ±0.38 1.00 ±0.15 galactonate-1,4- 0.76 ±0.14 0.21 ±0.16 0.29 ±0.11 0.33 ±0.83 1.00 ±0.19 lactone galactose 0.40 ±0.56 0.09 ±0.26 0.12 ±0.26 0.13 ±0.56 1.00 ±0.15 galacturonate 0.97 ±0.08 0.44 ±0.30 0.54 ±0.11 0.46 ±0.34 1.00 ±0.18 glucose-6-P 0.68 ±0.22 0.51 ±0.08 0.58 ±0.07 0.78 ±0.37 1.00 ±0.47 gluconate 1.17 ±0.06 0.87 ±0.15 0.55 ±0.11 0.54 ±0.09 1.00 ±0.13 glucose 0.37 ±0.46 0.06 ±0.45 0.07 ±0.40 0.08 ±0.53 1.00 ±0.63 glutamate 0.91 ±0.08 0.81 ±0.23 1.03 ±0.05 1.23 ±0.07 1.00 ±0.04 glutamine 4 0.28 ±0.18 0.58 ±0.07 0.34 ±0.32 0.47 ±0.51 1.00 ±0.39 glycerate 1.20 ±0.15 0.97 ±0.14 1.11 ±0.11 1.26 ±0.16 1.00 ±0.23 glycerate-3-P 0.92 ±0.22 0.93 ±0.19 0.96 ±0.05 1.66 ±0.16 1.00 ±0.27 glycerol 0.88 ±0.29 0.92 ±0.11 0.69 ±0.21 0.88 ±0.42 1.00 ±0.14 glycerol-1-P 1.08 ±0.18 0.99 ±0.08 0.80 ±0.07 0.72 ±0.11 1.00 ±0.17 glycine 0.44 ±0.10 0.48 ±0.21 0.24 ±0.13 0.34 ±0.49 1.00 ±0.10 homoserine 0.75 ±0.16 0.53 ±0.13 0.37 ±0.25 0.32 ±0.46 1.00 ±0.13 inositol 1.00 ±0.10 0.58 ±0.12 1.16 ±0.07 1.11 ±0.25 1.00 ±0.22 inositol-1-P 1.32 ±0.05 0.75 ±0.04 1.34 ±0.11 0.92 ±0.27 1.00 ±0.16 isocitrate 1.57 ±0.05 1.10 ±0.11 1.63 ±0.14 1.39 ±0.29 1.00 ±0.21 isoleucine 0.30 ±0.30 0.22 ±0.18 0.18 ±0.15 0.23 ±0.38 1.00 ±0.10 L-ascorbate 1.12 ±0.18 1.00 ±0.12 1.13 ±0.19 0.86 ±0.27 1.00 ±0.07 leucine 0.57 ±0.18 0.59 ±0.31 0.28 ±0.15 0.26 ±0.12 1.00 ±0.21 lysine 0.45 ±0.15 0.62 ±0.14 0.32 ±0.11 0.44 ±0.35 1.00 ±0.19 malate 0.63 ±0.21 0.24 ±0.20 0.27 ±0.19 0.21 ±0.50 1.00 ±0.25 maleate 0.81 ±0.29 0.54 ±0.31 0.39 ±0.37 0.36 ±0.70 1.00 ±0.27 maltose 1.02 ±0.28 0.50 ±0.13 0.36 ±0.16 0.44 ±0.55 1.00 ±0.14 mannitol 0.64 ±0.04 0.46 ±0.05 0.39 ±0.22 0.58 ±0.38 1.00 ±0.16 mannose 0.73 ±0.44 0.15 ±0.18 0.17 ±0.23 0.25 ±0.86 1.00 ±0.29 melezitose 1.33 ±0.04 0.87 ±0.10 1.50 ±0.12 1.29 ±0.28 1.00 ±0.16 methionine 0.72 ±0.18 0.88 ±0.25 0.62 ±0.32 0.86 ±0.49 1.00 ±0.13 ornithine 0.51 ±0.12 0.83 ±0.21 0.53 ±0.25 0.66 ±0.33 1.00 ±0.14 phenylalanine 0.62 ±0.15 1.05 ±0.11 0.78 ±0.16 0.87 ±0.33 1.00 ±0.19 phosphate 1.48 ±0.15 0.90 ±0.17 1.42 ±0.07 1.31 ±0.25 1.00 ±0.14 proline 0.29 ±0.16 0.45 ±0.43 0.16 ±0.32 0.15 ±0.18 1.00 ±0.55 putrescine 1.73 ±0.09 1.43 ±0.06 1.27 ±0.06 1.21 ±0.21 1.00 ±0.19 quinate 1.78 ±0.09 1.18 ±0.10 0.59 ±0.08 0.62 ±0.56 1.00 ±0.11 raffinose 0.59 ±0.06 0.24 ±0.16 0.19 ±0.14 0.22 ±0.62 1.00 ±0.16 saccharate 1.32 ±0.20 1.31 ±0.09 1.11 ±0.09 1.08 ±0.33 1.00 ±0.12 serine 1.07 ±0.21 0.88 ±0.41 0.51 ±0.32 0.18 ±0.23 1.00 ±0.37 shikimate 0.74 ±0.11 0.79 ±0.13 0.54 ±0.13 3.99 ±0.80 1.00 ±0.19 sorbitol/galactitol 0.67 ±0.10 0.61 ±0.20 0.79 ±0.13 0.96 ±0.41 1.00 ±0.23 spermidine 0.85 ±0.31 1.06 ±0.09 1.05 ±0.10 1.15 ±0.13 1.00 ±0.04 succinate 2.01 ±0.19 0.43 ±0.25 0.21 ±0.36 0.10 ±1.21 1.00 ±0.23 sucrose 1.47 ±0.15 0.56 ±0.24 0.65 ±0.17 0.31 ±0.30 1.00 ±0.17 t-4-HO-proline 0.50 ±0.16 0.65 ±0.29 0.53 ±0.26 0.42 ±1.15 1.00 ±0.24 threonate 0.99 ±0.05 0.75 ±0.06 0.82 ±0.13 0.58 ±0.15 1.00 ±0.10 threonine 1.21 ±0.34 2.21 ±0.50 0.75 ±0.17 0.67 ±0.18 1.00 ±0.11 trehalose 1.00 ±0.28 0.46 ±0.08 0.61 ±0.16 0.83 ±0.32 1.00 ±0.27 tryptophan 0.79 ±0.30 1.51 ±0.29 0.83 ±0.23 0.82 ±0.23 1.00 ±0.33 tyramine 1.09 ±0.12 0.99 ±0.24 1.66 ±0.24 1.06 ±0.38 1.00 ±0.24 tyrosine 0.55 ±0.08 1.14 ±0.15 0.67 ±0.15 1.33 ±0.51 1.00 ±0.31 valine 0.60 ±0.10 0.70 ±0.17 0.27 ±0.32 0.35 ±0.43 1.00 ±0.04 xylose/arabinose 0.63 ±0.28 0.16 ±0.36 0.09 ±0.23 0.08 ±0.84 1.00 ±0.21 (b) Potato transgenic lines INV SE SP SE 10 SE 3PGA 1.00 ±0.00 146.67 ±0.01 1.00 ±0.00 5-oxoproline 0.68 ±0.09 0.28 ±0.24 1.00 ±0.07 6-P-gluconate 556.67 ±0.17 206.67 ±0.10 1.00 ±0.00 α-ketoglutarate 1.00 ±0.00 4.67 ±0.04 1.00 ±0.00 alanine 2.08 ±0.10 1.29 ±0.01 1.00 ±0.12 arginine 2.11 ±0.16 3.63 ±0.08 1.00 ±0.10 asparagine 1.17 ±0.06 0.10 ±0.02 1.00 ±0.15 aspartate 1.20 ±0.02 0.93 ±0.03 1.00 ±0.11 β-alanine 0.84 ±0.05 1.00 ±0.05 1.00 ±0.11 citarte 1.03 ±0.06 1.32 ±0.02 1.00 ±0.03 cysteine 2.20 ±0.14 1.90 ±0.08 1.00 ±0.05 fructose-6-P 27.00 ±0.10 10.17 ±0.04 1.00 ±0.16 fructose 2.55 ±0.07 1.09 ±0.08 1.00 ±0.26 fumarate 0.23 ±0.06 0.11 ±0.00 1.00 ±0.30 GABA 1.42 ±0.05 2.09 ±0.05 1.00 ±0.07 galactinol 1.00 ±0.00 1.00 ±0.00 1.00 ±0.00 galactose 0.26 ±0.12 2.96 ±0.16 1.00 ±0.35 glucose-6-P 23.23 ±0.08 13.23 ±0.04 1.00 ±0.10 gluconate 66.67 ±0.10 1.00 ±0.00 1.00 ±0.00 glucose 5.11 ±0.11 0.01 ±0.16 1.00 ±0.45 glucoronate 1.00 ±0.00 1.00 ±0.00 1.00 ±0.00 glutamate 1.38 ±0.02 0.93 ±0.03 1.00 ±0.02 glutmine 0.43 ±0.33 0.10 ±0.20 1.00 ±0.14 glutarate 1.00 ±0.00 1.00 ±0.00 1.00 ±0.00 glycerate 6.33 ±0.06 15.33 ±0.15 1.00 ±0.05 glycerol 1.00 ±0.00 23.33 ±0.08 1.00 ±0.00 glycine 0.84 ±0.09 0.75 ±0.06 1.00 ±0.06 histidine 1.00 ±0.00 2083.33 ±0.12 1.00 ±0.00 homocysteine 1.00 ±0.00 4.67 ±0.14 1.00 ±0.00 homoglutamine 1.00 ±0.00 6.33 ±0.16 1.00 ±0.00 homoserine 0.50 ±0.21 0.50 ±0.08 1.00 ±0.10 inositol 0.21 ±0.08 0.18 ±0.04 1.00 ±0.14 isocitrate 0.67 ±0.12 0.90 ±0.02 1.00 ±0.03 isoleucine 1.16 ±0.14 0.93 ±0.15 1.00 ±0.06 isomaltose 13.33 ±0.14 1.00 ±0.00 1.00 ±0.00 L-ascorbate 0.73 ±0.33 0.68 ±0.07 1.00 ±0.26 leucine 1.70 ±0.17 1.21 ±0.15 1.00 ±0.12 lysine 0.62 ±0.19 2.22 ±0.09 1.00 ±0.04 malate 2.05 ±0.07 1.69 ±0.08 1.00 ±0.02 maltitol 586.67 ±0.14 1.00 ±0.00 1.00 ±0.00 maltose 8043.33 ±0.02 1.00 ±0.00 1.00 ±0.00 mannitol 2.94 ±0.06 1.46 ±0.04 1.00 ±0.04 mannose 10.18 ±0.10 0.05 ±0.00 1.00 ±0.30 methionine 0.84 ±0.10 1.21 ±0.06 1.00 ±0.05 norleucine 0.72 ±0.16 1.32 ±0.14 1.00 ±0.06 norvaline 0.58 ±0.10 1.03 ±0.07 1.00 ±0.07 ornithine 1.09 ±0.15 2.29 ±0.16 1.00 ±0.26 oxalate 1.00 ±0.00 1776.67 ±0.08 1.00 ±0.00 phenylalanine 1.77 ±0.07 1.47 ±0.02 1.00 ±0.07 phosphate 0.90 ±0.05 1.40 ±0.01 1.00 ±0.03 phosphoethanol 1.11 ±0.07 0.61 ±0.05 1.00 ±0.16 amine proline 0.82 ±0.09 0.59 ±0.05 1.00 ±0.03 quinate 1.42 ±0.02 1.84 ±0.08 1.00 ±0.08 raffinose 1.00 ±0.00 1.00 ±0.00 1.00 ±0.00 serine 3.12 ±0.05 1.90 ±0.01 1.00 ±0.09 shikimate 2.67 ±0.00 1.56 ±0.10 1.00 ±0.21 spermidine 2.10 ±0.05 2.30 ±0.06 1.00 ±0.14 succinate 2.23 ±0.01 1.10 ±0.07 1.00 ±0.25 sucrose 0.11 ±0.04 0.58 ±0.17 1.00 ±0.21 threonate 1.67 ±0.03 1.13 ±0.04 1.00 ±0.17 threonine 1.05 ±0.09 1.16 ±0.04 1.00 ±0.08 trehalose 193.33 ±0.14 1.00 ±0.00 1.00 ±0.00 tryptophan 266.67 ±0.33 1996.67 ±0.15 1.00 ±0.00 tyrosine 1.68 ±0.13 1.53 ±0.06 1.00 ±0.16 valine 0.90 ±0.10 0.53 ±0.06 1.00 ±0.02

TABLE 3 SPEAR- sig- EST ID ANNOTATION MB MAN 0.001 NOP CLEC13O19 HD-Zip protein [Arabidopsis thaliana] GABA 0.5430769 0 25 CLEC13O19 HD-Zip protein [Arabidopsis thaliana] INOSITOL −0.7853846 1 25 CLEC13O19 HD-Zip protein [Arabidopsis thaliana] SPERMIDINE 0.5892308 0 25 CLEC13O19 HD-Zip protein [Arabidopsis thaliana] TRYPTOPHAN 0.5913044 0 24 CLEC13O19 HD-Zip protein [Arabidopsis thaliana] TYROSINE 0.5638462 0 25 CLEC15K2 CCAAT box binding factor/transcription factor Hap2a {Arabidopsis GABA 0.5923077 0 25 thaliana}PIR|T49898|T49898 CCAAT CLEC15K2 CCAAT box binding factor/transcription factor Hap2a {Arabidopsis INOSITOL −0.7946154 1 25 thaliana}PIR|T49898|T49898 CCAAT CLEC15K2 CCAAT box binding factor/transcription factor Hap2a {Arabidopsis SPERMIDINE 0.6169231 0 25 thaliana}PIR|T49898|T49898 CCAAT CLEC15K2 CCAAT box binding factor/transcription factor Hap2a {Arabidopsis TRYPTOPHAN 0.6321739 1 24 thaliana}PIR|T49898|T49898 CCAAT CLEC15K2 CCAAT box binding factor/transcription factor Hap2a {Arabidopsis TYROSINE 0.5476923 0 25 thaliana}PIR|T49898|T49898 CCAAT CLEC21H24 osmotic stress-induced zinc-finger protein {Nicotiana GABA 0.5176923 0 25 tabacum}PIR|T01985|T01985 zinc-finger protein CLEC21H24 osmotic stress-induced zinc-finger protein {Nicotiana INOSITOL −0.7461538 1 25 tabacum}PIR|T01985|T01985 zinc-finger protein CLEC21H24 osmotic stress-induced zinc-finger protein {Nicotiana QUINATE 0.5338461 0 25 tabacum}PIR|T01985|T01985 zinc-finger protein CLEC21H24 osmotic stress-induced zinc-finger protein {Nicotiana SERINE 0.5053846 0 25 tabacum}PIR|T01985|T01985 zinc-finger protein CLEC21H24 osmotic stress-induced zinc-finger protein {Nicotiana SPERMIDINE 0.6 0 25 tabacum}PIR|T01985|T01985 zinc-finger protein CLEC21H24 osmotic stress-induced zinc-finger protein {Nicotiana TRYPTOPHAN 0.6026087 0 24 tabacum}PIR|T01985|T01985 zinc-finger protein CLEC21H24 osmotic stress-induced zinc-finger protein {Nicotiana TYROSINE 0.5592307 0 25 tabacum}PIR|T01985|T01985 zinc-finger protein CLEC28H13 homeodomain protein {Malus x domestica} GABA 0.5084615 0 25 CLEC28H13 homeodomain protein {Malus x domestica} SPERMIDINE 0.5938461 0 25 CLEC29A19 alanine aminotransferase {Arabidopsis thaliana} INOSITOL −0.7061539 1 25 CLEC29A19 alanine aminotransferase {Arabidopsis thaliana} SPERMIDINE 0.5715384 0 25 CLEC29A19 alanine aminotransferase {Arabidopsis thaliana} TRYPTOPHAN 0.5208696 0 24 CLEC32P10 putative C3HC4-type RING zinc finger protein {Arabidopsis GABA 0.5238461 0 25 thaliana}PIR|B84813|B84813 probable RING CLEC32P10 putative C3HC4-type RING zinc finger protein {Arabidopsis INOSITOL −0.5276923 0 25 thaliana}PIR|B84813|B84813 probable RING CLEC35G8 CYTOCHROME P450 83B1 (EC 1.14.—.—).GP|3164126|dbj|BAA28531.1|| INOSITOL −0.5130769 0 25 D78598 cytochrome P450 monooxygenase CLEC35G8 CYTOCHROME P450 83B1 (EC 1.14.—.—).GP|3164126|dbj|BAA28531.1|| SPERMIDINE 0.5207692 0 25 D78598 cytochrome P450 monooxygenase CLEC36G5 hydroxycinnamoyl-CoA:tyramine N-(hydroxycinnamoyl)transferase {Capsicum INOSITOL −0.7607692 1 25 annuum} CLEC36G5 hydroxycinnamoyl-CoA:tyramine N-(hydroxycinnamoyl)transferase {Capsicum MELEZITOSE −0.6210526 0 19 annuum} CLEC36G5 hydroxycinnamoyl-CoA:tyramine N-(hydroxycinnamoyl)transferase {Capsicum TYROSINE 0.6007692 0 25 annuum} CLEC38H15 NADH-dependent glutamate synthase {Arabidopsis thaliana} TYROSINE −0.5807692 0 25 CLEC39M7 NADH-dependent glutamate synthase {Arabidopsis thaliana} CITRAMALATE 0.5754386 0 19 CLEC40C16 ethylene-responsive transcriptional coactivator GABA 0.5492308 0 25 CLEC40C16 ethylene-responsive transcriptional coactivator INOSITOL −0.81 1 25 CLEC40C16 ethylene-responsive transcriptional coactivator MELEZITOSE −0.5929825 0 19 CLEC40C16 ethylene-responsive transcriptional coactivator SPERMIDINE 0.6330769 1 25 CLEC40C16 ethylene-responsive transcriptional coactivator THREONATE 0.5338461 0 25 CLEC40C16 ethylene-responsive transcriptional coactivator THREONINE 0.5539131 0 24 CLEC40C16 ethylene-responsive transcriptional coactivator TRYPTOPHAN 0.5443478 0 24 CLEC40C16 ethylene-responsive transcriptional coactivator TYROSINE 0.6223077 1 25 CLEC4A12 hydroxycinnamoyl-CoA:tyramine N-(hydroxycinnamoyl)transferase {Capsicum CYSTEINE 0.5385376 0 23 annuum} CLEC4A12 hydroxycinnamoyl-CoA:tyramine N-(hydroxycinnamoyl)transferase {Capsicum INOSITOL −0.6476923 1 25 annuum} CLEC4A12 hydroxycinnamoyl-CoA:tyramine N-(hydroxycinnamoyl)transferase {Capsicum LYSINE 0.5092308 0 25 annuum} CLEC4A12 hydroxycinnamoyl-CoA:tyramine N-(hydroxycinnamoyl)transferase {Capsicum MELEZITOSE −0.6210526 0 19 annuum} CLEC4A12 hydroxycinnamoyl-CoA:tyramine N-(hydroxycinnamoyl)transferase {Capsicum TYROSINE 0.5592307 0 25 annuum} CLEC6D16 glucosyltransferase-like protein {Arabidopsis thaliana} INOSITOL −0.5807692 0 25 CLEC6K9 lysine-ketoglutarate reductase/saccharopine dehydrogenase bifunctional enzyme INOSITOL −0.5907692 0 25 {Arabidopsis thaliana} CLEC6K9 lysine-ketoglutarate reductase/saccharopine dehydrogenase bifunctional enzyme SPERMIDINE 0.5407692 0 25 {Arabidopsis thaliana} CLEC6K9 lysine-ketoglutarate reductase/saccharopine dehydrogenase bifunctional enzyme TYROSINE 0.5076923 0 25 {Arabidopsis thaliana} CLED11B1 homeodomain protein INOSITOL −0.6515385 1 25 CLED11B1 homeodomain protein SPERMIDINE 0.6030769 0 25 CLED11B1 homeodomain protein TYROSINE 0.62 1 25 CLED11B18 lysine-ketoglutarate reductase/saccharopine dehydrogenase bifunctional enzyme GABA 0.5669231 0 25 {Arabidopsis thaliana} CLED11B18 lysine-ketoglutarate reductase/saccharopine dehydrogenase bifunctional enzyme INOSITOL −0.6469231 1 25 {Arabidopsis thaliana} CLED11B18 lysine-ketoglutarate reductase/saccharopine dehydrogenase bifunctional enzyme SPERMIDINE 0.5830769 0 25 {Arabidopsis thaliana} CLED11B18 lysine-ketoglutarate reductase/saccharopine dehydrogenase bifunctional enzyme THREONATE 0.5084615 0 25 {Arabidopsis thaliana} CLED11B18 lysine-ketoglutarate reductase/saccharopine dehydrogenase bifunctional enzyme TYROSINE 0.5184615 0 25 {Arabidopsis thaliana} CLED11B9 cytochrome p450 lxxia4 {Solanum melongena}SP|P37117|C714_SOLME INOSITOL −0.6653846 1 25 CYTOCHROME P450 71A4 (EC 1.14.—.—) ( CLED11B9 cytochrome p450 lxxia4 {Solanum melongena}SP|P37117|C714_SOLME TYROSINE 0.52 0 25 CYTOCHROME P450 71A4 (EC 1.14.—.—) ( CLED15E8 putative homeodomain transcription factor {Arabidopsis GABA 0.5846154 0 25 thaliana}PIR|H84774|H84774 probable homeodom CLED15E8 putative homeodomain transcription factor {Arabidopsis INOSITOL −0.7115384 1 25 thaliana}PIR|H84774|H84774 probable homeodom CLED15E8 putative homeodomain transcription factor {Arabidopsis SPERMIDINE 0.6315385 1 25 thaliana}PIR|H84774|H84774 probable homeodom CLED15E8 putative homeodomain transcription factor {Arabidopsis TRYPTOPHAN 0.546087 0 24 thaliana}PIR|H84774|H84774 probable homeodom CLED15E8 putative homeodomain transcription factor {Arabidopsis TYROSINE 0.5507692 0 25 thaliana}PIR|H84774|H84774 probable homeodom CLED15J6 Zn finger protein {Nicotiana tabacum}GP|1360078|emb|CAA66601.1|| INOSITOL −0.5330769 0 25 X97942 Zn finger protein {Nicotiana CLED16D1 NADH-ubiquinone oxidoreductase 20 kDa subunit precursor {Solanum INOSITOL −0.7161539 1 25 tuberosum}SP|Q43844|NUKM_SOLTU NAD CLED16D1 NADH-ubiquinone oxidoreductase 20 kDa subunit precursor {Solanum MELEZITOSE −0.6385965 0 19 tuberosum}SP|Q43844|NUKM_SOLTU NAD CLED16D1 NADH-ubiquinone oxidoreductase 20 kDa subunit precursor {Solanum SPERMIDINE 0.56 0 25 tuberosum}SP|Q43844|NUKM_SOLTU NAD CLED16D1 NADH-ubiquinone oxidoreductase 20 kDa subunit precursor {Solanum THREONINE 0.5391304 0 24 tuberosum}SP|Q43844|NUKM_SOLTU NAD CLED16D1 NADH-ubiquinone oxidoreductase 20 kDa subunit precursor {Solanum TYROSINE 0.6338462 1 25 tuberosum}SP|Q43844|NUKM_SOLTU NAD CLED21K4 “putative ABC transporter; 60211-54925 {Arabidopsis thaliana}PIR|E96742| INOSITOL 0.6238462 1 25 E96742 probable ABC transpor” CLED21K4 “putative ABC transporter; 60211-54925 {Arabidopsis thaliana}PIR|E96742| SPERMIDINE −0.5253846 0 25 E96742 probable ABC transpor” CLED21K4 “putative ABC transporter; 60211-54925 {Arabidopsis thaliana}PIR|E96742| TYROSINE −0.5892308 0 25 E96742 probable ABC transpor” CLED22C14 bHLH transcription factor GBOF-1 {Tulipa gesneriana} GABA 0.5623077 0 25 CLED22C14 bHLH transcription factor GBOF-1 {Tulipa gesneriana} INOSITOL −0.53 0 25 CLED24N6 acetylornithine aminotransferase precursor {Alnus INOSITOL −0.7492307 1 25 glutinosa}SP|O04866|ARGD_ALNGL ACETYLORNITHINE AM CLED24N6 acetylornithine aminotransferase precursor {Alnus MELEZITOSE −0.6631579 0 19 glutinosa}SP|O04866|ARGD_ALNGL ACETYLORNITHINE AM CLED24N6 acetylornithine aminotransferase precursor {Alnus SPERMIDINE 0.5492308 0 25 glutinosa}SP|O04866|ARGD_ALNGL ACETYLORNITHINE AM CLED24N6 acetylornithine aminotransferase precursor {Alnus TRYPTOPHAN 0.5547826 0 24 glutinosa}SP|O04866|ARGD_ALNGL ACETYLORNITHINE AM CLED24N6 acetylornithine aminotransferase precursor {Alnus TYROSINE 0.5884615 0 25 glutinosa}SP|O04866|ARGD_ALNGL ACETYLORNITHINE AM CLED25E6 UDP-glucose: salicylic acid glucosyltransferase {Nicotiana tabacum} INOSITOL −0.5915385 0 25 CLED25E6 UDP-glucose: salicylic acid glucosyltransferase {Nicotiana tabacum} SPERMIDINE 0.5253846 0 25 CLED28H13 putative cytochrome P450 {Solanum chacoense}SP|P93530|C7D6_SOLCH INOSITOL −0.5284615 0 25 CYTOCHROME P450 71D6 (EC 1.14.—.—) CLED28H13 putative cytochrome P450 {Solanum chacoense}SP|P93530|C7D6_SOLCH MELEZITOSE −0.577193 0 19 CYTOCHROME P450 71D6 (EC 1.14.—.—) CLED28N11 Dof zinc finger protein {Arabidopsis INOSITOL −0.6361538 1 25 thaliana}GP|9280230|dbj|BAB01720.1||AB023045 Dof zinc finger p CLED28N11 Dof zinc finger protein {Arabidopsis TYROSINE 0.5415385 0 25 thaliana}GP|9280230|dbj|BAB01720.1||AB023045 Dof zinc finger p CLED30B19 flavanone 3-hydroxylase-like protein {Arabidopsis thaliana} INOSITOL −0.5384616 0 25 CLED30B19 flavanone 3-hydroxylase-like protein {Arabidopsis thaliana} TYROSINE 0.5107692 0 25 CLED30J21 S-adenosylmethionine: 2-demethylmenaquinone methyltransferase-like protein INOSITOL −0.6807692 1 25 {Arabidopsis thaliana} CLED30J21 S-adenosylmethionine: 2-demethylmenaquinone methyltransferase-like protein SPERMIDINE 0.6107692 0 25 {Arabidopsis thaliana} CLED30J21 S-adenosylmethionine: 2-demethylmenaquinone methyltransferase-like protein SUCROSE −0.5191304 0 24 {Arabidopsis thaliana} CLED30J21 S-adenosylmethionine: 2-demethylmenaquinone methyltransferase-like protein TYROSINE 0.6738461 1 25 {Arabidopsis thaliana} CLED30M20 putative homeodomain transcription factor {Arabidopsis GABA 0.5469231 0 25 thaliana}PIR|H84774|H84774 probable homeodom CLED30M20 putative homeodomain transcription factor {Arabidopsis INOSITOL −0.7423077 1 25 thaliana}PIR|H84774|H84774 probable homeodom CLED30M20 putative homeodomain transcription factor {Arabidopsis NORLEUCINE −0.9428571 0 6 thaliana}PIR|H84774|H84774 probable homeodom CLED30M20 putative homeodomain transcription factor {Arabidopsis ORNITHINE −1 1 6 thaliana}PIR|H84774|H84774 probable homeodom CLED30M20 putative homeodomain transcription factor {Arabidopsis SERINE 0.5069231 0 25 thaliana}PIR|H84774|H84774 probable homeodom CLED30M20 putative homeodomain transcription factor {Arabidopsis SPERMIDINE 0.6007692 0 25 thaliana}PIR|H84774|H84774 probable homeodom CLED30M20 putative homeodomain transcription factor {Arabidopsis THREONATE 0.5438461 0 25 thaliana}PIR|H84774|H84774 probable homeodom CLED30M20 putative homeodomain transcription factor {Arabidopsis TRYPTOPHAN 0.5191304 0 24 thaliana}PIR|H84774|H84774 probable homeodom CLED30M20 putative homeodomain transcription factor {Arabidopsis TYROSINE 0.6215385 1 25 thaliana}PIR|H84774|H84774 probable homeodom CLED34H6 glucosyltransferase-like protein {Arabidopsis thaliana} FUCOSE −0.5807018 0 19 CLED34H6 glucosyltransferase-like protein {Arabidopsis thaliana} GALACTOSE −0.5846154 0 25 CLED34H6 glucosyltransferase-like protein {Arabidopsis thaliana} INOSITOL −0.6592308 1 25 CLED34H6 glucosyltransferase-like protein {Arabidopsis thaliana} SPERMIDINE 0.5346154 0 25 CLED34H6 glucosyltransferase-like protein {Arabidopsis thaliana} TRYPTOPHAN 0.56 0 24 CLED34H6 glucosyltransferase-like protein {Arabidopsis thaliana} TYROSINE 0.5176923 0 25 CLED4O17 putative cytochrome P450 {Solanum chacoense}SP|P93530|C7D6_SOLCH GABA 0.5346154 0 25 CYTOCHROME P450 71D6 (EC 1.14.—.—) CLED4O17 putative cytochrome P450 {Solanum chacoense}SP|P93530|C7D6_SOLCH INOSITOL −0.67 1 25 CYTOCHROME P450 71D6 (EC 1.14.—.—) CLED4O9 transcription factor CRC {Arabidopsis INOSITOL −0.5423077 0 25 thaliana}GP|12325076|gb|AAG52485.1|AC018364_3|AC018364 transc CLED5L18 “ornithine carbamoyltransferase; OCTase {Canavalia CYSTEINE 0.5306324 0 23 lineata}GP|12003188|gb|AAG43481.1|AF203688_1|AF20” CLED5L18 “ornithine carbamoyltransferase; OCTase {Canavalia FA 16:0 −0.6305469 0 18 lineata}GP|12003188|gb|AAG43481.1|AF203688_1|AF20” CLED5L18 “ornithine carbamoyltransferase; OCTase {Canavalia GABA 0.5630769 0 25 lineata}GP|12003188|gb|AAG43481.1|AF203688_1|AF20” CLED5L18 “ornithine carbamoyltransferase; OCTase {Canavalia INOSITOL −0.7792308 1 25 lineata}GP|12003188|gb|AAG43481.1|AF203688_1|AF20” CLED5L18 “ornithine carbamoyltransferase; OCTase {Canavalia MELEZITOSE −0.6 0 19 lineata}GP|12003188|gb|AAG43481.1|AF203688_1|AF20” CLED5L18 “ornithine carbamoyltransferase; OCTase {Canavalia TRYPTOPHAN 0.7104348 1 24 lineata}GP|12003188|gb|AAG43481.1|AF203688_1|AF20” CLED5L18 “ornithine carbamoyltransferase; OCTase {Canavalia TYROSINE 0.5592307 0 25 lineata}GP|12003188|gb|AAG43481.1|AF203688_1|AF20” CLED6K9 alpha-glucosidase {Solanum tuberosum subsp. tuberosum} THREONATE 0.5107692 0 25 CLED6P9 “ornithine carbamoyltransferase; OCTase {Canavalia ALANINE 0.5553846 0 25 lineata}GP|12003188|gb|AAG43481.1|AF203688_1|AF20” CLED6P9 “ornithine carbamoyltransferase; OCTase {Canavalia CYSTEINE 0.5375494 0 23 lineata}GP|12003188|gb|AAG43481.1|AF203688_1|AF20” CLED6P9 “ornithine carbamoyltransferase; OCTase {Canavalia INOSITOL −0.8292308 1 25 lineata}GP|12003188|gb|AAG43481.1|AF203688_1|AF20” CLED6P9 “ornithine carbamoyltransferase; OCTase {Canavalia LYSINE 0.5407692 0 25 lineata}GP|12003188|gb|AAG43481.1|AF203688_1|AF20” CLED6P9 “ornithine carbamoyltransferase; OCTase {Canavalia MELEZITOSE −0.7631579 1 19 lineata}GP|12003188|gb|AAG43481.1|AF203688_1|AF20” CLED6P9 “ornithine carbamoyltransferase; OCTase {Canavalia SERINE 0.5323077 0 25 lineata}GP|12003188|gb|AAG43481.1|AF203688_1|AF20” CLED6P9 “ornithine carbamoyltransferase; OCTase {Canavalia SPERMIDINE 0.5515385 0 25 lineata}GP|12003188|gb|AAG43481.1|AF203688_1|AF20” CLED6P9 “ornithine carbamoyltransferase; OCTase {Canavalia T-4-HO-PROLINE 0.6 0 19 lineata}GP|12003188|gb|AAG43481.1|AF203688_1|AF20” CLED6P9 “ornithine carbamoyltransferase; OCTase {Canavalia THREONATE 0.5176923 0 25 lineata}GP|12003188|gb|AAG43481.1|AF203688_1|AF20” CLED6P9 “ornithine carbamoyltransferase; OCTase {Canavalia THREONINE 0.5591304 0 24 lineata}GP|12003188|gb|AAG43481.1|AF203688_1|AF20” CLED6P9 “ornithine carbamoyltransferase; OCTase {Canavalia TRYPTOPHAN 0.5930435 0 24 lineata}GP|12003188|gb|AAG43481.1|AF203688_1|AF20” CLED6P9 “ornithine carbamoyltransferase; OCTase {Canavalia TYROSINE 0.6330769 1 25 lineata}GP|12003188|gb|AAG43481.1|AF203688_1|AF20” CLED7G23 Similar to acyl carrier protein, mitochondrial precursor (ACP) NADH-ubiquinone INOSITOL −0.6430769 1 25 oxidoreductase 9.6 KD CLED7G23 Similar to acyl carrier protein, mitochondrial precursor (ACP) NADH-ubiquinone MELEZITOSE −0.6157895 0 19 oxidoreductase 9.6 KD CLED8G16 DIACYLGLYCEROL KINASE 1 (EC 2.7.1.107) (DIGLYCERIDE KINASE) INOSITOL −0.5869231 0 25 (DGK 1) (DAG KINASE 1).GP|1374772|dbj|B CLEG12G7 cytochrome P450-like protein {Arabidopsis GABA 0.5992308 0 25 thaliana}GP|7270932|emb|CAB80611.1||AL161595 cytochrome P CLEG12G7 cytochrome P450-like protein {Arabidopsis INOSITOL −0.7884616 1 25 thaliana}GP|7270932|emb|CAB80611.1||AL161595 cytochrome P CLEG12G7 cytochrome P450-like protein {Arabidopsis SERINE 0.5430769 0 25 thaliana}GP|7270932|emb|CAB80611.1||AL161595 cytochrome P CLEG12G7 cytochrome P450-like protein {Arabidopsis SPERMIDINE 0.62 1 25 thaliana}GP|7270932|emb|CAB80611.1||AL161595 cytochrome P CLEG12G7 cytochrome P450-like protein {Arabidopsis TRYPTOPHAN 0.6226087 0 24 thaliana}GP|7270932|emb|CAB80611.1||AL161595 cytochrome P CLEG12G7 cytochrome P450-like protein {Arabidopsis TYROSINE 0.6115385 0 25 thaliana}GP|7270932|emb|CAB80611.1||AL161595 cytochrome P CLEG12O3 similar to ATPases associated with various cellular activites (Pfam: AAA.hmm, GABA 0.5638462 0 25 score: 230.91) {Arabid CLEG12O3 similar to ATPases associated with various cellular activites (Pfam: AAA.hmm, INOSITOL −0.7407692 1 25 score: 230.91) {Arabid CLEG12O3 similar to ATPases associated with various cellular activites (Pfam: AAA.hmm, SERINE 0.5238461 0 25 score: 230.91) {Arabid CLEG12O3 similar to ATPases associated with various cellular activites (Pfam: AAA.hmm, SPERMIDINE 0.6476923 1 25 score: 230.91) {Arabid CLEG12O3 similar to ATPases associated with various cellular activites (Pfam: AAA.hmm, TRYPTOPHAN 0.5869565 0 24 score: 230.91) {Arabid CLEG12O3 similar to ATPases associated with various cellular activites (Pfam: AAA.hmm, TYROSINE 0.5746154 0 25 score: 230.91) {Arabid CLEG16B16 succinate dehydrogenase flavoprotein alpha subunit {Arabidopsis GABA 0.5776923 0 25 thaliana}GP|8843734|dbj|BAA97282.1| CLEG16B16 succinate dehydrogenase flavoprotein alpha subunit {Arabidopsis INOSITOL −0.7607692 1 25 thaliana}GP|8843734|dbj|BAA97282.1| CLEG16B16 succinate dehydrogenase flavoprotein alpha subunit {Arabidopsis TYROSINE 0.6015385 0 25 thaliana}GP|8843734|dbj|BAA97282.1| CLEG27G1 putative NADH-ubiquinone oxireductase {Arabidopsis thaliana}PIR|C84588| GABA 0.6184615 1 25 C84588 probable NADH-ubiquin CLEG27G1 putative NADH-ubiquinone oxireductase {Arabidopsis thaliana}PIR|C84588| INOSITOL −0.7776923 1 25 C84588 probable NADH-ubiquin CLEG27G1 putative NADH-ubiquinone oxireductase {Arabidopsis thaliana}PIR|C84588| MALTITOL 0.9428571 0 6 C84588 probable NADH-ubiquin CLEG27G1 putative NADH-ubiquinone oxireductase {Arabidopsis thaliana}PIR|C84588| SERINE 0.5661538 0 25 C84588 probable NADH-ubiquin CLEG27G1 putative NADH-ubiquinone oxireductase {Arabidopsis thaliana}PIR|C84588| SPERMIDINE 0.6846154 1 25 C84588 probable NADH-ubiquin CLEG27G1 putative NADH-ubiquinone oxireductase {Arabidopsis thaliana}PIR|C84588| SUCROSE −0.5252174 0 24 C84588 probable NADH-ubiquin CLEG27G1 putative NADH-ubiquinone oxireductase {Arabidopsis thaliana}PIR|C84588| THREONATE 0.5207692 0 25 C84588 probable NADH-ubiquin CLEG27G1 putative NADH-ubiquinone oxireductase {Arabidopsis thaliana}PIR|C84588| TRYPTOPHAN 0.6008695 0 24 C84588 probable NADH-ubiquin CLEG27G1 putative NADH-ubiquinone oxireductase {Arabidopsis thaliana}PIR|C84588| TYROSINE 0.6153846 0 25 C84588 probable NADH-ubiquin CLEG28D24 76 kDa mitochondrial complex I subunit {Solanum GABA 0.5392308 0 25 tuberosum}SP|Q43644|NUAM_SOLTU NADH-UBIQUINONE OXID CLEG28D24 76 kDa mitochondrial complex I subunit {Solanum INOSITOL −0.6692308 1 25 tuberosum}SP|Q43644|NUAM_SOLTU NADH-UBIQUINONE OXID CLEG28D24 76 kDa mitochondrial complex I subunit {Solanum SERINE 0.5392308 0 25 tuberosum}SP|Q43644|NUAM_SOLTU NADH-UBIQUINONE OXID CLEG28D24 76 kDa mitochondrial complex I subunit {Solanum SPERMIDINE 0.5761539 0 25 tuberosum}SP|Q43644|NUAM_SOLTU NADH-UBIQUINONE OXID CLEG28D24 76 kDa mitochondrial complex I subunit {Solanum TRYPTOPHAN 0.5182609 0 24 tuberosum}SP|Q43644|NUAM_SOLTU NADH-UBIQUINONE OXID CLEG30O13 phosphate/phosphoenolpyruvate translocator protein-like {Arabidopsis thaliana} GABA 0.5876923 0 25 CLEG30O13 phosphate/phosphoenolpyruvate translocator protein-like {Arabidopsis thaliana} INOSITOL −0.7707692 1 25 CLEG30O13 phosphate/phosphoenolpyruvate translocator protein-like {Arabidopsis thaliana} QUINATE 0.5076923 0 25 CLEG30O13 phosphate/phosphoenolpyruvate translocator protein-like {Arabidopsis thaliana} SPERMIDINE 0.6084616 0 25 CLEG30O13 phosphate/phosphoenolpyruvate translocator protein-like {Arabidopsis thaliana} TRYPTOPHAN 0.6147826 0 24 CLEG32P19 glucosyl transferase {Nicotiana tabacum}GP|1805359|dbj|BAA19155.1|| GABA 0.6169231 0 25 AB000623 glucosyl transferase {N CLEG32P19 glucosyl transferase {Nicotiana tabacum}GP|1805359|dbj|BAA19155.1|| INOSITOL −0.5876923 0 25 AB000623 glucosyl transferase {N CLEG32P19 glucosyl transferase {Nicotiana tabacum}GP|1805359|dbj|BAA19155.1|| SPERMIDINE 0.5246154 0 25 AB000623 glucosyl transferase {N CLEG33A5 w-3 desaturase {Solanum tuberosum}PIR|T07685|T07685 omega-3 fatty acid GABA 0.5238461 0 25 desaturase (EC 1.14.99.—)- CLEG33A5 w-3 desaturase {Solanum tuberosum}PIR|T07685|T07685 omega-3 fatty acid INOSITOL −0.6038461 0 25 desaturase (EC 1.14.99.—)- CLEG33O5 NADH-ubiquinone oxidoreductase 20 kDa subunit precursor {Solanum INOSITOL −0.7030769 1 25 tuberosum}SP|Q43844|NUKM_SOLTU NAD CLEG33O5 NADH-ubiquinone oxidoreductase 20 kDa subunit precursor {Solanum SERINE 0.523077 0 25 tuberosum}SP|Q43844|NUKM_SOLTU NAD CLEG33O5 NADH-ubiquinone oxidoreductase 20 kDa subunit precursor {Solanum SPERMIDINE 0.5138462 0 25 tuberosum}SP|Q43844|NUKM_SOLTU NAD CLEG33O5 NADH-ubiquinone oxidoreductase 20 kDa subunit precursor {Solanum THREONATE 0.51 0 25 tuberosum}SP|Q43844|NUKM_SOLTU NAD CLEG33O5 NADH-ubiquinone oxidoreductase 20 kDa subunit precursor {Solanum TYROSINE 0.6584615 1 25 tuberosum}SP|Q43844|NUKM_SOLTU NAD CLEG35I11 putative homeodomain transcription factor {Arabidopsis GABA 0.5915385 0 25 thaliana}PIR|F84565|F84565 probable homeodom CLEG35I11 putative homeodomain transcription factor {Arabidopsis INOSITOL −0.7892308 1 25 thaliana}PIR|F84565|F84565 probable homeodom CLEG35I11 putative homeodomain transcription factor {Arabidopsis SPERMIDINE 0.5415385 0 25 thaliana}PIR|F84565|F84565 probable homeodom CLEG35I11 putative homeodomain transcription factor {Arabidopsis TRYPTOPHAN 0.5634782 0 24 thaliana}PIR|F84565|F84565 5 probable homeodom CLEG35I11 putative homeodomain transcription factor {Arabidopsis TYROSINE 0.5907692 0 25 thaliana}PIR|F84565|F84565 probable homeodom CLEG37C14 zinc finger protein-like {Arabidopsis thaliana} GABA 0.5523077 0 25 CLEG37C14 zinc finger protein-like {Arabidopsis thaliana} INOSITOL −0.8192308 1 25 CLEG37C14 zinc finger protein-like {Arabidopsis thaliana} MELEZITOSE −0.654386 0 19 CLEG37C14 zinc finger protein-like {Arabidopsis thaliana} SPERMIDINE 0.5746154 0 25 CLEG37C14 zinc finger protein-like {Arabidopsis thaliana} TRYPTOPHAN 0.5721739 0 24 CLEG37C14 zinc finger protein-like {Arabidopsis thaliana} TYROSINE 0.6707692 1 25 CLEG39L11 transcription factor TEIL {Nicotiana tabacum} INOSITOL −0.5953846 0 25 CLEG39N19 dehydroquinate dehydratase/shikimate:NADP oxidoreductase GABA 0.54 0 25 CLEG39N19 dehydroquinate dehydratase/shikimate:NADP oxidoreductase INOSITOL −0.7023077 1 25 CLEG39N23 dTDP-glucose 4-6-dehydratases-like protein {Arabidopsis INOSITOL −0.5907692 0 25 thaliana}PIR|T45701|T45701 dTDP-glucose 4-6 CLEG3E11 glycerol-3-phosphate dehydrogenase {Arabidopsis thaliana}PIR|F84832|F84832 INOSITOL −0.5938461 0 25 glycerol-3-phosphate deh CLEG41L23 phosphate/phosphoenolpyruvate translocator protein-like {Arabidopsis thaliana} GABA 0.56 0 25 CLEG41L23 phosphate/phosphoenolpyruvate translocator protein-like {Arabidopsis thaliana} INOSITOL −0.74 1 25 CLEG41L23 phosphate/phosphoenolpyruvate translocator protein-like {Arabidopsis thaliana} SERINE 0.5653846 0 25 CLEG41L23 phosphate/phosphoenolpyruvate translocator protein-like {Arabidopsis thaliana} SPERMIDINE 0.63 1 25 CLEG41L23 phosphate/phosphoenolpyruvate translocator protein-like {Arabidopsis thaliana} TRYPTOPHAN 0.5660869 0 24 CLEG41L23 phosphate/phosphoenolpyruvate translocator protein-like {Arabidopsis thaliana} TYROSINE 0.5246154 0 25 CLEG41P2 delta 1-pyrroline-5-carboxylate synthetase 3PGA −0.9428571 0 6 CLEG41P2 delta 1-pyrroline-5-carboxylate synthetase A- −1 1 5 KETOGLUTARATE CLEG41P2 delta 1-pyrroline-5-carboxylate synthetase GABA 0.5092308 0 25 CLEG41P2 delta 1-pyrroline-5-carboxylate synthetase INOSITOL −0.7530769 1 25 CLEG41P2 delta 1-pyrroline-5-carboxylate synthetase SPERMIDINE 0.5492308 0 25 CLEG41P2 delta 1-pyrroline-5-carboxylate synthetase THREONATE 0.5107692 0 25 CLEG41P2 delta 1-pyrroline-5-carboxylate synthetase TYROSINE 0.6723077 1 25 CLEG42N24 “putative ABC transporter; 73228-76244 {Arabidopsis thaliana}” INOSITOL −0.59 0 25 CLEG43E15 CCAAT box binding factor/transcription factor Hap2a {Arabidopsis GABA 0.5469231 0 25 thaliana}PIR|T49898|T49898 CCAAT CLEG43E15 CCAAT box binding factor/transcription factor Hap2a {Arabidopsis INOSITOL −0.5330769 0 25 thaliana}PIR|T49898|T49898 CCAAT CLEG43N9 sugar-phosphate isomerase-like protein {Arabidopsis thaliana}PIR|T47628| INOSITOL −0.5153846 0 25 T47628 sugar-phosphate isom CLEG8L3 similar to ATPases associated with various cellular activites (Pfam: AAA.hmm, GABA 0.6207692 1 25 score: 230.91) {Arabid CLEG8L3 similar to ATPases associated with various cellular activites (Pfam: AAA.hmm, GALACTOSE −0.5215384 0 25 score: 230.91) {Arabid CLEG8L3 similar to ATPases associated with various cellular activites (Pfam: AAA.hmm, INOSITOL −0.7284616 1 25 score: 230.91) {Arabid CLEG8L3 similar to ATPases associated with various cellular activites (Pfam: AAA.hmm, SPERMIDINE 0.6807692 1 25 score: 230.91) {Arabid CLEG8L3 similar to ATPases associated with various cellular activites (Pfam: AAA.hmm, SUCROSE −0.5478261 0 24 score: 230.91) {Arabid CLEG8L3 similar to ATPases associated with various cellular activites (Pfam: AAA.hmm, TRYPTOPHAN 0.5669565 0 24 score: 230.91) {Arabid CLEG8L3 similar to ATPases associated with various cellular activites (Pfam: AAA.hmm, TYROSINE 0.5715384 0 25 score: 230.91) {Arabid CLEG9A20 alanine aminotransferase {Arabidopsis thaliana} GABA 0.5507692 0 25 CLEG9A20 alanine aminotransferase {Arabidopsis thaliana} INOSITOL −0.6023077 0 25 CLEG9A20 alanine aminotransferase {Arabidopsis thaliana} SPERMIDINE 0.5392308 0 25 CLEG9A20 alanine aminotransferase {Arabidopsis thaliana} THREONATE 0.5561538 0 25 CLEI11O22 acetylornithine aminotransferase precursor {Alnus GABA 0.5930769 0 25 glutinosa}SP|O04866|ARGD_ALNGL ACETYLORNITHINE AM CLEI11O22 acetylornithine aminotransferase precursor {Alnus INOSITOL −0.77 1 25 glutinosa}SP|O04866|ARGD_ALNGL ACETYLORNITHINE AM CLEI11O22 acetylornithine aminotransferase precursor {Alnus SERINE 0.52 0 25 glutinosa}SP|O04866|ARGD_ALNGL ACETYLORNITHINE AM CLEI11O22 acetylornithine aminotransferase precursor {Alnus SPERMIDINE 0.6461539 1 25 glutinosa}SP|O04866|ARGD_ALNGL ACETYLORNITHINE AM CLEI11O22 acetylornithine aminotransferase precursor {Alnus TRYPTOPHAN 0.6017391 0 24 glutinosa}SP|O04866|ARGD_ALNGL ACETYLORNITHINE AM CLEI11O22 acetylornithine aminotransferase precursor {Alnus TYROSINE 0.5607693 0 25 glutinosa}SP|O04866|ARGD_ALNGL ACETYLORNITHINE AM CLEI12O14 fructose-6-phosphate 2-kinase/fructose-2,6-bisphosphatase {Solanum GABA 0.51 0 25 tuberosum}PIR|T07016|T07016 6-ph CLEI12O14 fructose-6-phosphate 2-kinase/fructose-2,6-bisphosphatase {Solanum INOSITOL −0.7807692 1 25 tuberosum}PIR|T07016|T07016 6-ph CLEI12O14 fructose-6-phosphate 2-kinase/fructose-2,6-bisphosphatase {Solanum MELEZITOSE −0.5947368 0 19 tuberosum}PIR|T07016|T07016 6-ph CLEI12O14 fructose-6-phosphate 2-kinase/fructose-2,6-bisphosphatase {Solanum SERINE 0.5692308 0 25 tuberosum}PIR|T07016|T07016 6-ph CLEI12O14 fructose-6-phosphate 2-kinase/fructose-2,6-bisphosphatase {Solanum SPERMIDINE 0.5907692 0 25 tuberosum}PIR|T07016|T07016 6-ph CLEI12O14 fructose-6-phosphate 2-kinase/fructose-2,6-bisphosphatase {Solanum TRYPTOPHAN 0.5469565 0 24 tuberosum}PIR|T07016|T07016 6-ph CLEI12O14 fructose-6-phosphate 2-kinase/fructose-2,6-bisphosphatase {Solanum TYROSINE 0.6484615 1 25 tuberosum}PIR|T07016|T07016 6-ph CLEI13J17 TRYPTOPHAN SYNTHASE BETA CHAIN 2 PRECURSOR (EC GABA 0.6007692 0 25 4.2.1.20).GP|2792520|gb|AAB97087.1||AF042320 tryptop CLEI13J17 TRYPTOPHAN SYNTHASE BETA CHAIN 2 PRECURSOR (EC INOSITOL −0.7107692 1 25 4.2.1.20).GP|2792520|gb|AAB97087.1||AF042320 tryptop CLEI13J17 TRYPTOPHAN SYNTHASE BETA CHAIN 2 PRECURSOR (EC SPERMIDINE 0.6561539 1 25 4.2.1.20).GP|2792520|gb|AAB97087.1||AF042320 tryptop CLEI13J17 TRYPTOPHAN SYNTHASE BETA CHAIN 2 PRECURSOR (EC TYROSINE 0.5876923 0 25 4.2.1.20).GP|2792520|gb|AAB97087.1||AF042320 tryptop CLEI15M10 fructose-6-phosphate 2-kinase/fructose-2,6-bisphosphatase {Solanum INOSITOL −0.7076923 1 25 tuberosum}PIR|T07016|T07016 6-ph CLEI15M10 fructose-6-phosphate 2-kinase/fructose-2,6-bisphosphatase {Solanum THREONINE 0.5286956 0 24 tuberosum}PIR|T07016|T07016 6-ph CLEI15M10 fructose-6-phosphate 2-kinase/fructose-2,6-bisphosphatase {Solanum TYROSINE 0.6469231 1 25 tuberosum}PIR|T07016|T07016 6-ph CLEI5A6 transcription factor WRKY6 {Arabidopsis ALANINE 0.5330769 0 25 thaliana}GP|12658412|gb|AAK01128.1|AF331713_1|AF331713 tran CLEI5A6 transcription factor WRKY6 {Arabidopsis INOSITOL −0.7923077 1 25 thaliana}GP|12658412|gb|AAK01128.1|AF331713_1|AF331713 tran CLEI5A6 transcription factor WRKY6 {Arabidopsis LYSINE 0.5076923 0 25 thaliana}GP|12658412|gb|AAK01128.1|AF331713_1|AF331713 tran CLEI5A6 transcription factor WRKY6 {Arabidopsis SERINE 0.6246154 1 25 thaliana}GP|12658412|gb|AAK01128.1|AF331713_1|AF331713 tran CLEI5A6 transcription factor WRKY6 {Arabidopsis SPERMIDINE 0.6038461 0 25 thaliana}GP|12658412|gb|AAK01128.1|AF331713_1|AF331713 tran CLEI5A6 transcription factor WRKY6 {Arabidopsis THREONATE 0.5107692 0 25 thaliana}GP|12658412|gb|AAK01128.1|AF331713_1|AF331713 tran CLEI5A6 transcription factor WRKY6 {Arabidopsis THREONINE 0.5156522 0 24 thaliana}GP|12658412|gb|AAK01128.1|AF331713_1|AF331713 tran CLEI5A6 transcription factor WRKY6 {Arabidopsis TYROSINE 0.6753846 1 25 thaliana}GP|12658412|gb|AAK01128.1|AF331713_1|AF331713 tran CLEL16O9 Similar to Populus balsamifera subsp. trichocarpa X Populus deltoides vegetative SORBITOL/ 0.7058824 0 17 storage protein. (L GALACTITOL CLEM17A5 bHLH transcription factor GBOF-1 {Tulipa gesneriana} 3PGA 0.9428571 0 6 CLEM17A5 bHLH transcription factor GBOF-1 {Tulipa gesneriana} GABA 0.5769231 0 25 CLEM17A5 bHLH transcription factor GBOF-1 {Tulipa gesneriana} INOSITOL −0.6176923 0 25 CLEM17A5 bHLH transcription factor GBOF-1 {Tulipa gesneriana} MANNOSE −0.5855449 0 22 CLEM19M11 ADP-glucose pyrophosphorylase small subunit INOSITOL −0.5384616 0 25 CLEM21P8 dehydroquinate dehydratase/shikimate:NADP oxidoreductase INOSITOL −0.6807692 1 25 CLEM21P8 dehydroquinate dehydratase/shikimate:NADP oxidoreductase SERINE 0.5269231 0 25 CLEM21P8 dehydroquinate dehydratase/shikimate:NADP oxidoreductase SPERMIDINE 0.6407692 1 25 CLEM21P8 dehydroquinate dehydratase/shikimate:NADP oxidoreductase THREONATE 0.5538462 0 25 CLEM21P8 dehydroquinate dehydratase/shikimate:NADP oxidoreductase THREONATE 0.5373913 0 24 CLEM23I12 SNAP25A protein {Arabidopsis thaliana}GP|5731763|emb|CAB52582.1||X92419 GABA 0.6192307 1 25 SNAP25A protein {Arabidopsi CLEM23I12 SNAP25A protein {Arabidopsis thaliana}GP|5731763|emb|CAB52582.1||X92419 INOSITOL −0.6284615 1 25 SNAP25A protein {Arabidopsi CLEM23I12 SNAP25A protein {Arabidopsis thaliana}GP|5731763|emb|CAB52582.1||X92419 SPERMIDINE 0.6623077 1 25 SNAP25A protein {Arabidopsi CLEM23I12 SNAP25A protein {Arabidopsis thaliana}GP|5731763|emb|CAB52582.1||X92419 SUCROSE −0.5834783 0 24 SNAP25A protein {Arabidopsi CLEM23I12 SNAP25A protein {Arabidopsis thaliana}GP|5731763|emb|CAB52582.1||X92419 TYROSINE 0.6146154 0 25 SNAP25A protein {Arabidopsi CLEM3K4 URIDYLATE KINASE (EC 2.7.4.—) (UK) (URIDINE MONOPHOSPHATE GABA 0.5107692 0 25 KINASE) (UMP KINASE) (UMP/CMP KINASE).GP| CLEM3K4 URIDYLATE KINASE (EC 2.7.4.—) (UK) (URIDINE MONOPHOSPHATE INOSITOL −0.7507693 1 25 KINASE) (UMP KINASE) (UMP/CMP KINASE).GP| CLEM3K4 URIDYLATE KINASE (EC 2.7.4.—) (UK) (URIDINE MONOPHOSPHATE SPERMIDINE 0.5130769 0 25 KINASE) (UMP KINASE) (UMP/CMP KINASE).GP| CLEM3K4 URIDYLATE KINASE (EC 2.7.4.—) (UK) (URIDINE MONOPHOSPHATE TYROSINE 0.6261538 1 25 KINASE) (UMP KINASE) (UMP/CMP KINASE).GP| CLEM4L3 TRYPTOPHAN SYNTHASE BETA CHAIN 2 PRECURSOR (EC ALANINE 0.5161539 0 25 4.2.1.20).GP|2792520|gb|AAB97087.1||AF042320 tryptop CLEM4L3 TRYPTOPHAN SYNTHASE BETA CHAIN 2 PRECURSOR (EC GABA 0.5569231 0 25 4.2.1.20).GP|2792520|gb|AAB97087.1||AF042320 tryptop CLEM4L3 TRYPTOPHAN SYNTHASE BETA CHAIN 2 PRECURSOR (EC INOSITOL −0.8246154 1 25 4.2.1.20).GP|2792520|gb|AAB97087.1||AF042320 tryptop CLEM4L3 TRYPTOPHAN SYNTHASE BETA CHAIN 2 PRECURSOR (EC MELEZITOSE −0.6087719 0 19 4.2.1.20).GP|2792520|gb|AAB97087.1||AF042320 tryptop CLEM4L3 TRYPTOPHAN SYNTHASE BETA CHAIN 2 PRECURSOR (EC SPERMIDINE 0.5569231 0 25 4.2.1.20).GP|2792520|gb|AAB97087.1||AF042320 tryptop CLEM4L3 TRYPTOPHAN SYNTHASE BETA CHAIN 2 PRECURSOR (EC TRYPTOPHAN 0.6104348 0 24 4.2.1.20).GP|2792520|gb|AAB97087.1||AF042320 tryptop CLEM4L3 TRYPTOPHAN SYNTHASE BETA CHAIN 2 PRECURSOR (EC TYROSINE 0.6469231 1 25 4.2.1.20).GP|2792520|gb|AAB97087.1||AF042320 tryptop CLEM8E24 glucose-6-phosphate 1-dehydrogenase {Solanum TYRAMINE 0.620227 0 18 tuberosum}SP|P37830|G6PD_SOLTU GLUCOSE-6-PHOSPHATE 1-D CLEN21M4 “putative ABC transporter; 73228-76244 {Arabidopsis thaliana}” GABA 0.6323077 1 25 CLEN21M4 “putative ABC transporter; 73228-76244 {Arabidopsis thaliana}” INOSITOL −0.7407692 1 25 CLEN21M4 “putative ABC transporter; 73228-76244 {Arabidopsis thaliana}” SPERMIDINE 0.6023077 0 25 CLEN21M4 “putative ABC transporter; 73228-76244 {Arabidopsis thaliana}” TRYPTOPHAN 0.6095652 0 24 CLER2B1 serine/threonine-specific protein kinase NAK {Arabidopsis INOSITOL −0.5807692 0 25 thaliana}PIR|T48250|T48250 serine/threoni CLES16N17 ADP-glucose pyrophosphorylase small subunit INOSITOL −0.7192308 1 25 CLES16N17 ADP-glucose pyrophosphorylase small subunit SERINE 0.52 0 25 CLES16N17 ADP-glucose pyrophosphorylase small subunit THREONINE 0.5434783 0 24 CLES16N17 ADP-glucose pyrophosphorylase small subunit TYROSINE 0.6161538 0 25 CLES20P12 putative cytochrome P450 INOSITOL −0.5369231 0 25 CLES20P12 putative cytochrome P450 MELEZITOSE −0.6 0 19 CLET10A17 SNAP25A protein {Arabidopsis thaliana}GP|5731763|emb|CAB52582.1||X92419 GABA 0.5892308 0 25 SNAP25A protein {Arabidopsi CLET10A17 SNAP25A protein {Arabidopsis thaliana}GP|5731763|emb|CAB52582.1||X92419 INOSITOL −0.7292308 1 25 SNAP25A protein {Arabidopsi CLET10A17 SNAP25A protein {Arabidopsis thaliana}GP|5731763|emb|CAB52582.1||X92419 SPERMIDINE 0.6638461 1 25 SNAP25A protein {Arabidopsi CLET10A17 SNAP25A protein {Arabidopsis thaliana}GP|5731763|emb|CAB52582.1||X92419 SUCROSE −0.5313044 0 24 SNAP25A protein {Arabidopsi CLET10A17 SNAP25A protein {Arabidopsis thaliana}GP|5731763|emb|CAB52582.1||X92419 TRYPTOPHAN 0.5469565 0 24 SNAP25A protein {Arabidopsi CLET10A17 SNAP25A protein {Arabidopsis thaliana}GP|5731763|emb|CAB52582.1||X92419 TYROSINE 0.6376923 1 25 SNAP25A protein {Arabidopsi CLET12C14 MYB-like DNA-binding protein {Catharanthus roseus} INOSITOL −0.5492308 0 25 CLET12C14 MYB-like DNA-binding protein {Catharanthus roseus} TYROSINE 0.5630769 0 25 CLET1B18 CYTOCHROME P450 83B1 (EC 1.14.—.—).GP|3164126|dbj|BAA28531.1|| INOSITOL −0.5192308 0 25 D78598 cytochrome P450 monooxygenase CLET27N17 Similar to gb|AF135422 GDP-mannose pyrophosphorylase A (GMPPA) from INOSITOL −0.7669231 1 25 Homo sapiens. ESTs gb|AA712990, CLET27N17 Similar to gb|AF135422 GDP-mannose pyrophosphorylase A (GMPPA) from MELEZITOSE −0.5807018 0 19 Homo sapiens. ESTs gb|AA712990, CLET27N17 Similar to gb|AF135422 GDP-mannose pyrophosphorylase A (GMPPA) from SPERMIDINE 0.5946154 0 25 Homo sapiens. ESTs gb|AA712990, CLET27N17 Similar to gb|AF135422 GDP-mannose pyrophosphorylase A (GMPPA) from THREONINE 0.5156522 0 24 Homo sapiens. ESTs gb|AA712990, CLET27N17 Similar to gb|AF135422 GDP-mannose pyrophosphorylase A (GMPPA) from TYROSINE 0.6815385 1 25 Homo sapiens. ESTs gb|AA712990, CLET38C16-1 76 kDa mitochondrial complex I subunit {Solanum GABA 0.5223077 0 25 tuberosum}SP|Q43644|NUAM_SOLTU NADH-UBIQUINONE OXID CLET38C16-1 76 kDa mitochondrial complex I subunit {Solanum GALACTOSE −0.5384616 0 25 tuberosum}SP|Q43644|NUAM_SOLTU NADH-UBIQUINONE OXID CLET38C16-1 76 kDa mitochondrial complex I subunit {Solanum INOSITOL −0.6223077 1 25 tuberosum}SP|Q43644|NUAM_SOLTU NADH-UBIQUINONE OXID CLET38C16-1 76 kDa mitochondrial complex I subunit {Solanum SPERMIDINE 0.5884615 0 25 tuberosum}SP|Q43644|NUAM_SOLTU NADH-UBIQUINONE OXID CLET8H21 MADS-box transcription factor FBP21 {Petunia x hybrida} GABA 0.5430769 0 25 CLET8H21 MADS-box transcription factor FBP21 {Petunia x hybrida} INOSITOL −0.6869231 1 25 CLET8H21 MADS-box transcription factor FBP21 {Petunia x hybrida} SPERMIDINE 0.5669231 0 25 CLEW18G10 tyrosine aminotransferase-like protein {Arabidopsis thaliana} HOMOGLUTAMINE 1 1 5 CLEX11K13 Putative UDP-glucose glucosyltransferase {Arabidopsis GABA 0.6376923 1 25 thaliana}PIR|H86356|H86356 probable UDP-gluco CLEX11K13 Putative UDP-glucose glucosyltransferase {Arabidopsis INOSITOL −0.7146154 1 25 thaliana}PIR|H86356|H86356 probable UDP-gluco CLEX11K13 Putative UDP-glucose glucosyltransferase {Arabidopsis NORLEUCINE −0.9428571 0 6 thaliana}PIR|H86356|H86356 probable UDP-gluco CLEX11K13 Putative UDP-glucose glucosyltransferase {Arabidopsis NORVALINE −1 1 6 thaliana}PIR|H86356|H86356 probable UDP-gluco CLEX11K13 Putative UDP-glucose glucosyltransferase {Arabidopsis SERINE 0.5130769 0 25 thaliana}PIR|H86356|H86356 probable UDP-gluco CLEX11K13 Putative UDP-glucose glucosyltransferase {Arabidopsis SPERMIDINE 0.6784616 1 25 thaliana}PIR|H86356|H86356 probable UDP-gluco CLEX11K13 Putative UDP-glucose glucosyltransferase {Arabidopsis SUCROSE −0.5669565 0 24 thaliana}PIR|H86356|H86356 probable UDP-gluco CLEX11K13 Putative UDP-glucose glucosyltransferase {Arabidopsis THREONATE 0.51 0 25 thaliana}PIR|H86356|H86356 probable UDP-gluco CLEX11K13 Putative UDP-glucose glucosyltransferase {Arabidopsis TRYPTOPHAN 0.5443478 0 24 thaliana}PIR|H86356|H86356 probable UDP-gluco CLEX11K13 Putative UDP-glucose glucosyltransferase {Arabidopsis TYROSINE 0.5792308 0 25 thaliana}PIR|H86356|H86356 probable UDP-gluco CLEX11L22 PROBABLE VACUOLAR ATP SYNTHASE SUBUNIT F (EC 3.6.1.34) INOSITOL −0.7223077 1 25 (V-ATPASE F SUBUNIT) (VACUOLAR PROTON PUMP F CLEX11L22 PROBABLE VACUOLAR ATP SYNTHASE SUBUNIT F (EC 3.6.1.34) TYROSINE 0.5707693 0 25 (V-ATPASE F SUBUNIT) (VACUOLAR PROTON PUMP F CLEX11O7 transaldolase GALACTOSE 0.5407692 0 25 CLEX12A9 putative C3HC4-type RING zinc finger protein {Arabidopsis GABA 0.5323077 0 25 thaliana}PIR|B84813|B84813 probable RING CLEX12A9 putative C3HC4-type RING zinc finger protein {Arabidopsis INOSITOL −0.6253846 1 25 thaliana}PIR|B84813|B84813 probable RING CLEX12A9 putative C3HC4-type RING zinc finger protein {Arabidopsis SPERMIDINE 0.5715384 0 25 thaliana}PIR|B84813|B84813 probable RING CLEX13P4 Putative UDP-glucose glucosyltransferase {Arabidopsis ALANINE 0.5069231 0 25 thaliana}PIR|H86356|H86356 probable UDP-gluco CLEX13P4 Putative UDP-glucose glucosyltransferase {Arabidopsis INOSITOL −0.7553846 1 25 thaliana}PIR|H86356|H86356 probable UDP-gluco CLEX13P4 Putative UDP-glucose glucosyltransferase {Arabidopsis MELEZITOSE −0.5982456 0 19 thaliana}PIR|H86356|H86356 probable UDP-gluco CLEX13P4 Putative UDP-glucose glucosyltransferase {Arabidopsis NORVALINE −0.9428571 0 6 thaliana}PIR|H86356|H86356 probable UDP-gluco CLEX13P4 Putative UDP-glucose glucosyltransferase {Arabidopsis SPERMIDINE 0.5538462 0 25 thaliana}PIR|H86356|H86356 probable UDP-gluco CLEX13P4 Putative UDP-glucose glucosyltransferase {Arabidopsis THREONATE 0.5784615 0 25 thaliana}PIR|H86356|H86356 probable UDP-gluco CLEX13P4 Putative UDP-glucose glucosyltransferase {Arabidopsis TYROSINE 0.6669231 1 25 thaliana}PIR|H86356|H86356 probable UDP-gluco CLEX14L9 alanine aminotransferase {Arabidopsis HISTIDINE −0.9428571 0 6 thaliana}GP|12325273|gb|AAG52580.1|AC016529_11|AC016529 putat CLEX14L9 alanine aminotransferase {Arabidopsis NORVALINE −0.9428571 0 6 thaliana}GP|12325273|gb|AAG52580.1|AC016529_11|AC016529 putat CLEX1M19 Similar to gb|AF135422 GDP-mannose pyrophosphorylase A (GMPPA) from GABA 0.5069231 0 25 Homo sapiens. ESTs gb|AA712990, CLEX1M19 Similar to gb|AF135422 GDP-mannose pyrophosphorylase A (GMPPA) from INOSITOL −0.7115384 1 25 Homo sapiens. ESTs gb|AA712990, CLEX1M19 Similar to gb|AF135422 GDP-mannose pyrophosphorylase A (GMPPA) from SPERMIDINE 0.5453846 0 25 Homo sapiens. ESTs gb|AA712990, CLEX1M19 Similar to gb|AF135422 GDP-mannose pyrophosphorylase A (GMPPA) from THREONATE 0.51 0 25 Homo sapiens. ESTs gb|AA712990, CLEX1M19 Similar to gb|AF135422 GDP-mannose pyrophosphorylase A (GMPPA) from TYROSINE 0.6276923 1 25 Homo sapiens. ESTs gb|AA712990, CLEX4M2 osmotic stress-induced zinc-finger protein {Nicotiana tabacum}PIR|T01985| GABA 0.5192308 0 25 T01985 zinc-finger protein CLEX4M2 osmotic stress-induced zinc-finger protein {Nicotiana tabacum}PIR|T01985| INOSITOL −0.7076923 1 25 T01985 zinc-finger protein. CLEX4M2 osmotic stress-induced zinc-finger protein {Nicotiana tabacum}PIR|T019855| SPERMIDINE 0.6207692 1 25 T01985 zinc-finger protein CLEX4M2 osmotic stress-induced zinc-finger protein {Nicotiana tabacum}PIR|T01985| SUCROSE −0.5252174 0 24 T01985 zinc-finger protein CLEX4M2 osmotic stress-induced zinc-finger protein {Nicotiana tabacum}PIR|T01985| TYROSINE 0.6 0 25 T01985 zinc-finger protein. CLEY14E21 ALTERNATIVE OXIDASE 1 PRECURSOR (EC 1.—.—.—). GABA 0.5761539 0 25 GP|558054|gb|AAC60576.1||S71335 alternative oxidase, A CLEY14E21 ALTERNATIVE OXIDASE 1 PRECURSOR (EC 1.—.—.—). INOSITOL −0.7169231 1 25 GP|558054|gb|AAC60576.1||S71335 alternative oxidase, A CLEY14E21 ALTERNATIVE OXIDASE 1 PRECURSOR (EC 1.—.—.—). SPERMIDINE 0.6607692 1 25 GP|558054|gb|AAC60576.1||S71335 alternative oxidase, A CLEY14E21 ALTERNATIVE OXIDASE 1 PRECURSOR (EC 1.—.—.—). SUCROSE −0.5208696 0 24 GP|558054|gb|AAC60576.1||S71335 alternative oxidase, A CLEY14E21 ALTERNATIVE OXIDASE 1 PRECURSOR (EC 1.—.—.—). TRYPTOPHAN 0.5808696 0 24 GP|558054|gb|AAC60576.1||S71335 alternative oxidase, A CLEY14E21 ALTERNATIVE OXIDASE 1 PRECURSOR (EC 1.—.—.—). TYROSINE 0.5215384 0 25 GP|558054|gb|AAC60576.1||S71335 alternative oxidase, A CLEY15E1 caffeoyl-CoA O-methyltransferase 5 {Nicotiana INOSITOL 0.6846154 1 25 tabacum}GP|1679853|emb|CAB05369.1||Z82982 caffeoyl-Co CLEY15E1 caffeoyl-CoA O-methyltransferase 5 {Nicotiana LYSINE −0.523077 0 25 tabacum}GP|1679853|emb|CAB05369.1||Z82982 caffeoyl-Co CLEY15E1 caffeoyl-CoA O-methyltransferase 5 {Nicotiana MELEZITOSE 0.6035088 0 19 tabacum}GP|1679853|emb|CAB05369.1||Z82982 caffeoyl-Co CLEY15E1 caffeoyl-CoA O-methyltransferase 5 {Nicotiana THREONINE −0.5452174 0 24 tabacum}GP|1679853|emb|CAB05369.1||Z82982 caffeoyl-Co CLEY15E1 caffeoyl-CoA O-methyltransferase 5 {Nicotiana TYROSINE −0.6915385 1 25 tabacum|GP|1679853|emb|CAB05369.1||Z82982 caffeoyl-Co CLEY15P13 ATP synthase delta' subunit, mitochondrial precursor {Ipomoea INOSITOL −0.7076923 1 25 batatas}SP|Q40089|ATP4_IPOBA ATP SYNT CLEY15P13 ATP synthase delta' subunit, mitochondrial precursor {Ipomoea SERINE 0.5469231 0 25 batatas}SP|Q40089|ATP4_IPOBA ATP SYNT CLEY15P13 ATP synthase delta' subunit, mitochondrial precursor {Ipomoea SPERMIDINE 0.58 0 25 batatas}SP|Q40089|ATP4_IPOBA ATP SYNT CLEY15P13 ATP synthase delta' subunit, mitochondrial precursor {Ipomoea TYROSINE 0.6646154 1 25 batatas}SP|Q40089|ATP4_IPOBA ATP SYNT CLEY19P11 sugar-phosphate isomerase-like protein {Arabidopsis thaliana}PIR|T47628| INOSITOL −0.7 1 25 T47628 sugar-phosphate isom CLEY19P11 sugar-phosphate isomerase-like protein {Arabidopsis thaliana}PIR|T47628| SPERMIDINE 0.5476923 0 25 T47628 sugar-phosphate isom CLEY19P11 sugar-phosphate isomerase-ilke protein {Arabidopsis thaliana}PIR|T47628| TYROSINE 0.6046154 0 25 T47628 sugar-phosphate isom CLEY24E3 mas-binding factor MBF2 = transcription factor TGA1a homolog {Solanum GABA 0.5469231 0 25 tuberosum = potatoes, root, Peptid CLEY24E3 mas-binding factor MBF2 = transcription factor TGA1a homolog {Solanum INOSITOL −0.6369231 1 25 tuberosum = potatoes, root, Peptid CLEY24E3 mas-binding factor MBF2 = transcription factor TGA1a homolog {Solanum SPERMIDINE 0.5169231 0 25 tuberosum = potatoes, root, Peptid CLEY24E3 mas-binding factor MBF2 = transcription factor TGA1a homolog {Solanum TYROSINE 0.5353846 0 25 tuberosum = potatoes, root, Peptid CLEY26B11 URIDYLATE KINASE (EC 2.7.4.—) (UK) (URIDINE MONOPHOSPHATE GABA 0.5061538 0 25 KINASE) (UMP KINASE) (UMP/CMP KINASE).GP| CLEY26B11 URIDYLATE KINASE (EC 2.7.4.—) (UK) (URIDINE MONOPHOSPHATE INOSITOL −0.8092307 1 25 KINASE) (UMP KINASE) (UMP/CMP KINASE).GP| CLEY26B11 URIDYLATE KINASE (EC 2.7.4.—) (UK) (URIDINE MONOPHOSPHATE MELEZITOSE −0.6315789 0 19 KINASE) (UMP KINASE) (UMP/CMP KINASE).GP| CLEY26B11 URIDYLATE KINASE (EC 2.7.4.—) (UK) (URIDINE MONOPHOSPHATE SPERMIDINE 0.5407692 0 25 KINASE) (UMP KINASE) (UMP/CMP KINASE).GP| CLEY26B11 URIDYLATE KINASE (EC 2.7.4.—) (UK) (URIDINE MONOPHOSPHATE TYROSINE 0.6523077 1 25 KINASE) (UMP KINASE) (UMP/CMP KINASE).GP| CLEY2E3 UDP-glucose dehydrogenase-like protein {Arabidopsis thaliana}PIR|T51527| GABA 0.5315385 0 25 T51527 UDP-glucose dehydrog CLEY2E3 UDP-glucose dehydrogenase-like protein {Arabidopsis thaliana}PIR|T51527| INOSITOL −0.6569231 1 25 T51527 UDP-glucose dehydrog CLEY2E3 UDP-glucose dehydrogenase-like protein {Arabidopsis thaliana}PIR|T51527| SPERMIDINE 0.5623077 0 25 T51527 UDP-glucose dehydrog CLEZ16P14 dTDP-glucose 4-6-dehydratases-like protein {Arabidopsis INOSITOL −0.7861539 1 25 thaliana}PIR|T45701|T45701 dTDP-glucose 4-6 CLEZ16P14 dTDP-glucose 4-6-dehydratases-like protein {Arabidopsis MELEZITOSE −0.6140351 0 19 thaliana}PIR|T45701|T45701 dTDP-glucose 4-6 CLEZ16P14 dTDP-glucose 4-6-dehydratases-like protein {Arabidopsis SERINE 0.5623077 0 25 thaliana}PIR|T45701|T45701 dTDP-glucose 4-6 CLEZ16P14 dTDP-glucose 4-6-dehydratases-like protein {Arabidopsis SPERMIDINE 0.6 0 25 thaliana}PIR|T45701|T45701 dTDP-glucose 4-6 CLEZ16P14 dTDP-glucose 4-6-dehydratases-like protein {Arabidopsis THREONINE 0.5278261 0 24 thaliana}PIR|T45701|T45701 dTDP-glucose 4-6 CLEZ16P14 dTDP-glucose 4-6-dehydratases-like protein {Arabidopsis TRYPTOPHAN 0.5365217 0 24 thaliana}PIR|T45701|T45701 dTDP-glucose 4-6 CLEZ16P14 dTDP-glucose 4-6-dehydratases-like protein {Arabidopsis TYROSINE 0.6453846 1 25 thaliana}PIR|T45701|T45701 dTDP-glucose 4-6 CLEZ17K21 contains similarity to RING zinc finger protein~gene_id: MBD2.14 {Arabidopsis INOSITOL −0.6253846 1 25 thaliana} CLEZ17K21 contains similarity to RING zinc finger protein~gene_id: MBD2.14 {Arabidopsis MELEZITOSE −0.5894737 0 19 thaliana} CLEZ17K21 contains similarity to RING zinc finger protein~gene_id: MBD2.14 {Arabidopsis TYROSINE 0.5907692 0 25 thaliana} CLEZ20E22 Similar to acyl carrier protein, mitochondrial precursor (ACP) NADH-ubiquinone GABA 0.5469231 0 25 oxidoreductase 9.6 KD CLEZ20E22 Similar to acyl carrier protein, mitochondrial precursor (ACP) NADH-ubiquinone INOSITOL −0.73 1 25 oxidoreductase 9.6 KD CLEZ20E22 Similar to acyl carrier protein, mitochondrial precursor (ACP) NADH-ubiquinone SPERMIDINE 0.5784615 0 25 oxidoreductase 9.6 KD CLEZ20E22 Similar to acyl carrier protein, mitochondrial precursor (ACP) NADH-ubiquinone TYROSINE 0.6161538 0 25 oxidoreductase 9.6 KD CLEZ20I22 caffeoyl-CoA O-methyltransferase 5 {Nicotiana GLYCERATE −0.5643478 0 24 tabacum}GP|1679853|emb|CAB05369.1||Z82982 caffeoyl-Co CLEZ20I22 caffeoyl-CoA O-methyltransferase 5 {Nicotiana INOSITOL 0.7376923 1 25 tabacum}GP|1679853|emb|CAB05369.1||Z82982 caffeoyl-Co CLEZ20I22 caffeoyl-CoA O-methyltransferase 5 {Nicotiana SPERMIDINE −0.56 0 25 tabacum}GP|1679853|emb|CAB05369.1||Z82982 caffeoyl-Co CLEZ20I22 caffeoyl-CoA O-methyltransferase 5 {Nicotiana SUCROSE 0.5834783 0 24 tabacum}GP|1679853|emb|CAB05369.1||Z82982 caffeoyl-Co CLEZ20I22 caffeoyl-CoA O-methyltransferase 5 {Nicotiana TRYPTOPHAN −0.5695652 0 24 tabacum}GP|1679853|emb|CAB05369.1||Z82982 caffeoyl-Co CLEZ20I22 caffeoyl-CoA O-methyltransferase 5 {Nicotiana TYROSINE −0.6776923 1 25 tabacum}GP|1679853|emb|CAB05369.1||Z82982 caffeoyl-Co CLEZ8J8 “putative transcription factor BTF3 (RNA polymerase B transcription factor 3); INOSITOL −0.7307692 1 25 26343-27201 {Arabidops” CLEZ8J8 “putative transcription factor BTF3 (RNA polymerase B transcription factor 3); THREONINE 0.5321739 0 24 26343-27201 {Arabidops” CLEZ8J8 “putative transcription factor BTF3 (RNA polymerase B transcription factor 3); TYROSINE 0.6807692 1 25 26343-27201 {Arabidops” CLEZ9G24 succinate dehydrogenase flavoprotein alpha subunit {Arabidopsis GABA 0.5692308 0 25 thaliana}GP|8843734|dbj|BAA97282.1| CLEZ9G24 succinate dehydrogenase flavoprotein alpha subunit {Arabidopsis INOSITOL −0.7292308 1 25 thaliana}GP|8843734|dbj|BAA97282.1| CLEZ9G24 succinate dehydrogenase flavoprotein alpha subunit {Arabidopsis SERINE 0.5738462 0 25 thaliana}GP|8843734|dbj|BAA97282.1| CLEZ9G24 succinate dehydrogenase flavoprotein alpha subunit {Arabidopsis SPERMIDINE 0.6384615 1 25 thaliana}GP|8843734|dbj|BAA97282.1| CLEZ9G24 succinate dehydrogenase flavoprotein alpha subunit {Arabidopsis THREONATE 0.5207692 0 25 thaliana}GP|8843734|dbj|BAA97282.1| CLEZ9G24 succinate dehydrogenase flavoprotein alpha subunit {Arabidopsis TYROSINE 0.5923077 0 25 thaliana}GP|8843734|dbj|BAA97282.1| CLHT18D23 TOM (target of myb1)-like protein {Arabidopsis thaliana}PIR|T51543|T51543 INOSITOL −0.6846154 1 25 TOM (target of myb1)-like CLHT18D23 TOM (target of myb1)-like protein {Arabidopsis thaliana}PIR|T51543|T51543 SERINE 0.5130769 0 25 TOM (target of myb1)-like CLHT18D23 TOM (target of myb1)-like protein {Arabidopsis thaliana}PIR|T51543|T51543 SPERMIDINE 0.64 1 25 TOM (target of myb1)-like CLHT18D23 TOM (target of myb1)-like protein {Arabidopsis thaliana}PIR|T51543|T51543 TYROSINE 0.5407692 0 25 TOM (target of myb1)-like CLHT23L11 cytochrome P450-like protein {Arabidopsis INOSITOL −0.6053846 0 25 thaliana}GP|7270932|emb|CAB80611.1||AL161595 cytochrome P CLHT31P20 glycolate oxidase {Arabidopsis thaliana} INOSITOL −0.5346154 0 25 CLHT31P20 glycolate oxidase {Arabidopsis thaliana} TYROSINE 0.5192308 0 25 CLHT6C11 w-3 desaturase {Solanum tuberosum}PIR|T07685|T07685 omega-3 fatty acid INOSITOL −0.75 1 25 desaturase (EC 1.14.99.—)- CLHT6C11 w-3 desaturase {Solanum tuberosum}PIR|T07685|T07685 omega-3 fatty acid LYSINE 0.5915385 0 25 desaturase (EC 1.14.99.—)- CLHT6C11 w-3 desaturase {Solanum tuberosum}PIR|T07685|T07685 omega-3 fatty acid MELEZITOSE −0.6070175 0 19 desaturase (EC 1.14.99.—)- CLHT6C11 w-3 desaturase {Solanum tuberosum}PIR|T07685|T07685 omega-3 fatty acid SPERMIDINE 0.5407692 0 25 desaturase (EC 1.14.99.—)- CLHT6C11 w-3 desaturase {Solanum tuberosum}PIR|T07685|T07685 omega-3 fatty acid TYROSINE 0.6907693 1 25 desaturase (EC 1.14.99.—)- CLHT6E15 TOM (target of myb1)-like protein {Arabidopsis thaliana}PIR|T51543|T51543 GABA 0.5215384 0 25 TOM (target of myb1)-like CLHT6E15 TOM (target of myb1)-like protein {Arabidopsis thaliana}PIR|T51543|T51543 INOSITOL −0.7238461 1 25 TOM (target of myb1)-like CLHT6E15 TOM (target of myb1)-like protein {Arabidopsis thaliana}PIR|T51543|T51543 SERINE 0.5638462 0 25 TOM (target of myb1)-like CLHT6E15 TOM (target of myb1)-like protein {Arabidopsis thaliana}PIR|T51543|T51543 SPERMIDINE 0.64 1 25 TOM (target of myb1)-like CLHT6E15 TOM (target of myb1)-like protein {Arabidopsis thaliana}PIR|T51543|T51543 THREONINE 0.5165218 0 24 TOM (target of myb1)-like CLHT6E15 TOM (target of myb1)-like protein {Arabidopsis thaliana}PIR|T51543|T51543 TYROSINE 0.6069231 0 25 TOM (target of myb1)-like CLPP11G6 putative monosaccharide transporter 1 {Petunia x hybrida} INOSITOL −0.5330769 0 25 CLPP11N17 sugar transporter like protein {Arabidopsis INOSITOL −0.5861539 0 25 thaliana}GP|2464913|emb|CAB16808.1||Z99708 sugar transp CLPP11N17 sugar transporter like protein {Arabidopsis MELEZITOSE −0.5842105 0 19 thaliana}GP|2464913|emb|CAB16808.1||Z99708 sugar transp CLPP13C23 fructokinase 1 {Arabidopsis INOSITOL −0.5376923 0 25 thaliana}GP|13878053|gb|AAK44104.1|AF370289_1|AF370289 putative fructok CLPP13M11 fructokinase 1 {Arabidopsis GABA 0.5292308 0 25 thaliana}GP|13878053|gb|AAK44104.1|AF370289_1|AF370289 putative fructok CLPP13M11 fructokinase 1 {Arabidopsis INOSITOL −0.5638462 0 25 thaliana}GP|13878053|gb|AAK44104.1|AF370289_1|AF370289 putative fructok CLPP2C18 ALTERNATIVE OXIDASE 1 PRECURSOR (EC 1.—.—.—). GABA 0.6276923 1 25 GP|558054|gb|AAC60576.1||S71335 alternative oxidase, A CLPP2C18 ALTERNATIVE OXIDASE 1 PRECURSOR (EC 1.—.—.—). INOSITOL −0.7538462 1 25 GP|558054|gb|AAC60576.1||S71335 alternative oxidase, A CLPP2C18 ALTERNATIVE OXIDASE 1 PRECURSOR (EC 1.—.—.—). SPERMIDINE 0.65 1 25 GP|558054|gb|AAC60576.1||S71335 alternative oxidase, A CLPP2C18 ALTERNATIVE OXIDASE 1 PRECURSOR (EC 1.—.—.—). TRYPTOPHAN 0.526087 0 24 GP|558054|gb|AAC60576.1||S71335 alternative oxidase, A CLPP2C18 ALTERNATIVE OXIDASE 1 PRECURSOR (EC 1.—.—.—). TYROSINE 0.5646154 0 25 GP|558054|gb|AAC60576.1||S71335 alternative oxidase, A CLPP5L24 glutamate decarboxylase isozyme 1 {Nicotiana tabacum} GABA 0.5592307 0 25 CLPP5L24 glutamate decarboxylase isozyme 1 {Nicotiana tabacum} INOSITOL −0.7623077 1 25 CLPP5L24 glutamate decarboxylase isozyme 1 {Nicotiana tabacum} MELEZITOSE −0.6140351 0 19 CLPP5L24 glutamate decarboxylase isozyme 1 {Nicotiana tabacum} SPERMIDINE 0.6376923 1 25 CLPP5L24 glutamate decarboxylase isozyme 1 {Nicotiana tabacum} THREONINE 0.5156522 0 24 CLPP5L24 glutamate decarboxylase isozyme 1 {Nicotiana tabacum} TRYPTOPHAN 0.5878261 0 24 CLPP5L24 glutamate decarboxylase isozyme 1 {Nicotiana tabacum} TYROSINE 0.6284615 1 25 CLPP8K20 phosphate/phosphoenolpyruvate translocator-like protein {Arabidopsis thaliana} INOSITOL −0.6984615 1 25 CLPP9C20 phosphate/phosphoenolpyruvate translocator-like protein {Arabidopsis thaliana} GABA 0.5584615 0 25 CLPP9C20 phosphate/phosphoenolpyruvate translocator-like protein {Arabidopsis thaliana} INOSITOL −0.6769231 1 25 CLPP9C20 phosphate/phosphoenolpyruvate translocator-like protein {Arabidopsis thaliana} SPERMIDINE 0.5523077 0 25 CLPP9O23 glutamate decarboxylase isozyme 1 {Nicotiana tabacum} GABA 0.6446154 1 25 CLPP9O23 glutamate decarboxylase isozyme 1 {Nicotiana tabacum} INOSITOL −0.6515385 1 25 CLPP9O23 glutamate decarboxylase isozyme 1 {Nicotiana tabacum} SPERMIDINE 0.6115385 0 25 CLPP9O23 glutamate decarboxylase isozyme 1 {Nicotiana tabacum} TYROSINE 0.5169231 0 25 CLPT10L12 glycogen (starch) synthase precursor {Solanum GABA 0.5923077 0 25 tuberosum}SP|Q00775|UGST_SOLTU GRANULE-BOUND GLYCOGEN CLPT10L12 glycogen (starch) synthase precursor {Solanum INOSITOL −0.7446154 1 25 tuberosum}SP|Q00775|UGST_SOLTU GRANULE-BOUND GLYCOGEN CLPT10L12 glycogen (starch) synthase precursor {Solanum NORVALINE −0.9428571 0 6 tuberosum}SP|Q00775|UGST_SOLTU GRANULE-BOUND GLYCOGEN CLPT10L12 glycogen (starch) synthase precursor {Solanum ORNITHINE −0.9428571 0 6 tuberosum}SP|Q00775|UGST_SOLTU GRANULE-BOUND GLYCOGEN CLPT10L12 glycogen (starch) synthase precursor {Solanum SPERMIDINE 0.5930769 0 25 tuberosum}SP|Q00775|UGST_SOLTU GRANULE-BOUND GLYCOGEN CLPT10L12 glycogen (starch) synthase precursor {Solanum SUCROSE −0.5582609 0 24 tuberosum}SP|Q00775|UGST_SOLTU GRANULE-BOUND GLYCOGEN CLPT10L12 glycogen (starch) synthase precursor {Solanum TRYPTOPHAN 0.5391304 0 24 tuberosum}SP|Q00775|UGST_SOLTU GRANULE-BOUND GLYCOGEN CLPT10L12 glycogen (starch) synthase precursor {Solanum TYROSINE 0.6007692 0 25 tuberosum}SP|Q00775|UGST_SOLTU GRANULE-BOUND GLYCOGEN CLPT11O16 putative ripening-related bZIP protein {Vitis vinifera} SORBITOL/ 0.627451 0 17 GALACTITOL CLPT5N10 aldose 1-epimerase-like protein {Arabidopsis thaliana} SORBITOL/ 0.6519608 0 17 GALACTITOL CLPT8B12 ARF GAP-like zinc finger-containing protein ZiGA4 {Arabidopsis thaliana} INOSITOL −0.5107692 0 25 CTOA19J6 cytochrome p450 lxxia4 {Solanum melongena}SP|P37117|C714_SOLME INOSITOL −0.5915385 0 25 CYTOCHROME P450 71A4 (EC 1.14.—.—) ( CTOA19J6 cytochrome p450 lxxia4 {Solanum melongena}SP|P37117|C714_SOLME TYROSINE 0.5215384 0 25 CYTOCHROME P450 71A4 (EC 1.14.—.—) ( CTOE12M9 flavanone 3-hydroxylase-like protein {Arabidopsis thaliana} GABA 0.5192308 0 25 CTOE12M9 flavanone 3-hydroxylase-like protein {Arabidopsis thaliana} INOSITOL −0.6238462 1 25 CTOE12M9 flavanone 3-hydroxylase-like protein {Arabidopsis thaliana} MANNOSE −0.608131 0 22 CTOE17L19 PROBABLE VACUOLAR ATP SYNTHASE SUBUNIT F (EC 3.6.1.34) GABA 0.5215384 0 25 (V-ATPASE F SUBUNIT) (VACUOLAR PROTON PUMP F CTOE17L19 PROBABLE VACUOLAR ATP SYNTHASE SUBUNIT F (EC 3.6.1.34) GALACTOSE −0.52 0 25 V-ATPASE F SUBUNIT) (VACUOLAR PROTON PUMP F CTOE17L19 PROBABLE VACUOLAR ATP SYNTHASE SUBUNIT F (EC 3.6.1.34) INOSITOL −0.6061538 0 25 (V-ATPASE F SUBUNIT) (VACUOLAR PROTON PUMP F CTOE17L19 PROBABLE VACUOLAR ATP SYNTHASE SUBUNIT F (EC 3.6.1.34) SPERMIDINE 0.6846154 1 25 (V-ATPASE F SUBUNIT) (VACUOLAR PROTON PUMP F CTOE17L19 PROBABLE VACUOLAR ATP SYNTHASE SUBUNIT F (EC 3.6.1.34) SUCROSE −0.5173913 0 24 (V-ATPASE F SUBUNIT) (VACUOLAR PROTON PUMP F CTOE17L19 PROBABLE VACUOLAR ATP SYNTHASE SUBUNIT F (EC 3.6.1.34) TYROSINE 0.56 0 25 (V-ATPASE F SUBUNIT) (VACUOLAR PROTON PUMP F CTOE2C17 delta 1-pyrroline-5-carboxylate synthetase INOSITOL −0.5315385 0 25 CTOE2C17 delta 1-pyrroline-5-carboxylate synthetase MANNOSE −0.5448899 0 22 CTOE2F5 putative cytochrome P450 GABA 0.5407692 0 25 CTOE2F5 putative cytochrome P450 INOSITOL −0.6776923 1 25 CTOE2F5 putative cytochrome P450 SPERMIDINE 0.6046154 0 25 CTOE2F5 putative cytochrome P450 TRYPTOPHAN 0.5226087 0 24 CTOE2F5 putative cytochrome P450 TYROSINE 0.5546154 0 25 CTOE6J10 transcription factor IIA small subunit {Arabidopsis INOSITOL −0.5969231 0 25 thaliana}GP|5051786|emb|CAB45079.1||AL078637 tr CTOE6J10 transcription factor IIA small subunit {Arabidopsis SPERMIDINE 0.5830769 0 25 thaliana}GP|5051786|emb|CAB45079.1||AL078637 tr CTOE6J10 transcription factor IIA small subunit {Arabidopsis THREONATE 0.5576923 0 25 thaliana}GP|5051786|emb|CAB45079.1||AL078637 tr CTOF10I1 ATP synthase delta' subunit, mitochondrial precursor {lpomoea INOSITOL −0.74 1 25 batatas}SP|Q40089|ATP4_IPOBA ATP SYNT CTOF10I1 ATP synthase delta' subunit, mitochondrial precursor {lpomoea MELEZITOSE −0.5807018 0 19 batatas}SP|Q40089|ATP4_IPOBA ATP SYNT CTOF10I1 ATP synthase delta' subunit, mitochondrial precursor {lpomoea SERINE 0.5107692 0 25 batatas}SP|Q40089|ATP4_IPOBA ATP SYNT CTOF10I1 ATP synthase delta' subunit, mitochondrial precursor {lpomoea SPERMIDINE 0.6292308 1 25 batatas}SP|Q40089|ATP4_IPOBA ATP SYNT CTOF10I1 ATP synthase delta' subunit, mitochondrial precursor {lpomoea TYROSINE 0.6846154 1 25 batatas}SP|Q40089|ATP4_IPOBA ATP SYNT CTOF10L8 S-adenosyl-L-methionine synthetase INOSITOL −0.6415384 1 25 CTOF10L8 S-adenosyl-L-methionine synthetase SPERMIDINE 0.6230769 1 25 CTOF10L8 S-adenosyl-L-methionine synthetase SUCROSE −0.5252174 0 24 CTOF10L8 S-adenosyl-L-methionine synthetase TYROSINE 0.6030769 0 25 CTOF14N18 small zinc finger-like protein INOSITOL −0.5153846 0 25 CTOF14N18 small zinc finger-like protein TYROSINE 0.5407692 0 25 CTOF19M22 zinc finger protein-like {Arabidopsis thaliana} INOSITOL −0.6023077 0 25 CTOF19M22 zinc finger protein-like {Arabidopsis thaliana} SPERMIDINE 0.5561538 0 25 CTOF19M22 zinc finger protein-like {Arabidopsis thaliana} TYROSINE 0.5707693 0 25 CTOF21A12 glycogen (starch) synthase precursor {Solanum INOSITOL −0.6869231 1 25 tuberosum}SP|Q00775|UGST_SOLTU GRANULE-BOUND GLYCOGEN CTOF21A12 glycogen (starch) synthase precursor {Solanum TYROSINE 0.6715385 1 25 tuberosum}SP|Q00775|UGST_SOLTU GRANULE-BOUND GLYCOGEN CTOF22G14 MYB-like DNA-binding protein {Catharanthus roseus} GABA 0.5807692 0 25 CTOF22G14 MYB-like DNA-binding protein {Catharanthus roseus} INOSITOL −0.7461538 1 25 CTOF22G14 MYB-like DNA-binding protein {Catharanthus roseus} SPERMIDINE 0.6292308 1 25 CTOF22G14 MYB-like DNA-binding protein {Catharanthus roseus} TYROSINE 0.6146154 0 25 CTOF23N20 “putative transcription factor BTF3 (RNA polymerase B transcription factor 3); INOSITOL −0.7276923 1 25 26343-27201 {Arabidops” CTOF23N20 “putative transcription factor BTF3 (RNA polymerase B transcription factor 3); TYROSINE 0.7007692 1 25 26343-27201 {Arabidops” CTOF25A17 small zinc finger-like protein MALTITOL 0.9428571 0 6 CTOF26K3 S-adenosylmethionine:2-demethylmenaquinone methyltransferase-like protein INOSITOL −0.5338461 0 25 {Arabidopsis thaliana} CTOF26K3 S-adenosylmethionine:2-demethylmenaquinone methyltransferase-like protein SPERMIDINE 0.5161539 0 25 {Arabidopsis thaliana} CTOF26K3 S-adenosylmethionine:2-demethylmenaquinone methyltransferase-like protein TYROSINE 0.5476923 0 25 {Arabidopsis thaliana} CTOF3J14 nucleotide diphosphate kinase la {Arabidopsis INOSITOL −0.5192308 0 25 thaliana}GP|6065740|emb|CAB58230.1||AJ012758 nucleoti CTOF3K21 S-adenosyl-L-methionine synthetase INOSITOL −0.6761538 1 25 CTOF3K21 S-adenosyl-L-methionine synthetase LYSINE 0.6038461 0 25 CTOF3K21 S-adenosyl-L-methionine synthetase TYROSINE 0.66 1 25 CTOF6M4 homeodomain protein INOSITOL −0.7223077 1 25 CTOF6M4 homeodomain protein SERINE 0.5592307 0 25 CTOF6M4 homeodomain protein SPERMIDINE 0.6046154 0 25 CTOF6M4 homeodomain protein THREONINE −0.5304348 0 24 CTOF6M4 homeodomain protein TYROSINE 0.6284615 1 25 CTOF7K11 cytochrome P450 like_TBP {Nicotiana GLYCEROL 0.5474308 0 23 tabacum}GP|1545805|dbj|BAA10929.1||D64052 cytochrome P450 like_(—) CTOF7K11 cytochrome P450 like_TBP {Nicotiana INOSITOL −0.5107692 0 25 tabacum}GP|1545805|dbj|BAA10929.1||D64052 cytochrome P450 like_(—) CTOF7K11 cytochrome P450 like_TBP {Nicotiana THREONINE 0.5252174 0 24 tabacum}GP|1545805|dbj|BAA10929.1||D64052 cytochrome P450 like_(—) CTOF7K11 cytochrome P450 like_TBP {Nicotiana TYROSINE 0.5446154 0 25 tabacum}GP|1545805|dbj|BAA10929.1||D64052 cytochrome P450 like_(—)

TABLE 4 Position for Position on Position on Position replicates Position on the filter the filter position on on Position on the 384 (primary (primary secondary secondary Description TC Accession No. Clone ID the 94-well plate wells-plate rows) columns) grid grid hexose transporter{circumflex over ( )}{circumflex over ( )}hexose transporter TC71791 AW040775 cLET10J17 XIC3 T3F5 R20 C6 r2-c1 r4-c3 protein{circumflex over ( )}{circumflex over ( )}pathogenesis-related protein P4{circumflex over ( )}{circumflex over ( )}pathogenesis-related protein PR1a (P4) 33 kDa precursor protein of oxygen-evolving complex TC71796 AW093398 cLET24B18 XIF6 T3L11 R14 C12 r2-c1 r4-c3 ADP-glucose pyrophosphorylase small subunit TC71797 BF050665 cLEM19M11 VIIH8 T2P15 R10 C16 r4-c2 r1-c3 utamine synthetase TC71798 AW626325 cLEZ19B18 XIVF2 T4K4 R21 C11 r2-c2 r1-c4 cytochrome P450 like_TBP {Nicotiana TC71805 BG124938 cTOF7K11 XXF12 T5L24 R1 C12 r3-c2 r4-c4 tabacum}GP|1545805|dbj|BAA10929.1||D64052 cytochrome P450 like_(—) fructose-bisphosphate aldolase {Persea americana} TC71818 AW931478 cLEZ7L12 XC3 T3E6 R19 C5 r2-c1 r4-c3 plastidic aldolase NPALDP1 {Nicotiana paniculata} TC71821 BG125770 cTOF9F8 XXIE8 T6I15 R12 C9 r3-c1 r2-c4 glutamate decarboxylase {Petunia TC71841 AW622545 cLEX15F21 XIIIC11 T4E21 R4 C5 r2-c2 r1-c4 hybrida}SP|Q07346|DCE_PETHY GLUTAMATE DECARBOXYLASE (EC 4.1.1.15) phenylalanine ammonia lyase TC71847 AI777201 cLER20L9 XB6 T3C12 R13 C3 r2-c1 r4-c3 glutamate decarboxylase isozyme 1 {Nicotiana TC71868 BG137392 cLPP5L24 XVF1 T4L1 R24 C12 r2-c2 r1-c4 tabacum} plastidic aldolase {Nicotiana paniculata} TC71875 AI781396 cLES15A20 XE1 T3I2 R23 C9 r2-c1 r4-c3 fructose-bisphosphate aldolase {Persea americana} TC71877 AW041348 cLET13N6 XID1 T3H1 R24 C8 r2-c1 r4-c3 ADENINE PHOSPHORIBOSYLTRANSFERASE 1 TC71878 AW092817 cLET22M4 XIF3 T3L5 R20 C12 r2-c1 r4-c3 (EC 2.4.2.7) (APRT).GP|16164|emb|CAA41497.1||X58640 adenine ph ribulose 1,5-bisphosphate carboxylase/oxygenase small TC71908 AW096400 cLET38B9 XXH6 T5P12 R13 C16 r3-c2 r4-c4 subunit{circumflex over ( )}{circumflex over ( )}ribulose 1,5-bisphosphate carboxylase/oxyenase ribulose-1,5-bisphosphate carboxylase, small subunit TC71912 AI776560 cLER19C5 IXH12 T3O23 R2 C15 r2-c1 r4-c3 precursor{circumflex over ( )}{circumflex over ( )}ribulose 1,5-bisphosphate carboxylase/oxygenase{circumflex over ( )}{circumflex over ( )}ribulose-1,5-bisphophate carboxylase/oxygenase small subunit phosphoribosyl diphosphate synthase {Arabidopsis TC71917 AI489108 cLED18D13 IIIB6 T1D11 R14 C4 r1-c2 r3-c3 thaliana}GP|4512664|gb|AAD21718.1||AC006931 putati glutamate dehydrogenase TC71919 AI782814 cLES20J18 XG9 T3M18 R7 C13 r2-c1 r4-c3 ribulose bisphosphate carboxylase small subunit 1 TC71926 BG124240 cTOF4F21 XXE4 T5J8 R17 C10 r3-c2 r4-c4 precursor {Lycopersicon esculentum}SP|P08706|RBS1 plastidic aldolase NPALDP1 {Nicotiana paniculata} TC71931 AW399700 cLPT8B16 XXID3 T6G5 R20 C7 r3-c1 r2-c4 spermine synthase 1 {Datura TC71984 AI779341 cLES7H6 XIA8 T3B15 R12 C2 r2-c1 r4-c3 stramonium}SP|Q96556|SPE1_DATST SPERMIDINE SYNTHASE 1 (EC 2.5.1.16) (PU glutamine synthetase {Lycopersicon esculentum} TC71994 BF098043 cLEW25C9 XIIG7 T3N14 R11 C14 r2-c1 r4-c3 glutamate decarboxylase isozyme 1 {Nicotiana TC71998 AW625683 cLEZ16B13 XIVD10 T4G20 R5 C7 r2-c2 r1-c4 tabacum} beta-fructosidase TC72004 AW222371 cLEN7H24 IXD5 T3G9 R16 C7 r2-c1 r4-c3 acid invertase, AI {EC 3.2.1.26} [Lycopersicon TC72005 BF112978 cLEG43E2 VIG1 T2M2 R23 C13 r4-c2 r1-c3 esculentum = tomatoes, cv. Super First, fruits, Peptide, 636 aa]{circumflex over ( )}{circumflex over ( )}vacuolar invertase precursor{circumflex over ( )}{circumflex over ( )}beta- fructofuranosidase beta-fructofuranosidase precursor {Lycopersicon TC72006 BE431852 cLEG4K9 VIH1 T2O2 R23 C15 r4-c2 r1-c3 esculentum}SP|P29000|INVA_LYCES ACID BETA- FRUCTOFUR beta-fructofuranosidase precursor {Lycopersicon TC72007 BE437004 cLEG35M1 VIC8 T2E16 R9 C5 r4-c2 r1-c3 esculentum}SP|P29000|INVA_LYCES ACID BETA- FRUCTOFUR enolase TC72015 BG131734 cTOE5I3 XXIA10 T6A19 R6 C1 r3-c1 r2-c4 threonine deaminase TC72016 AI488726 cLED13N11 IIH9 T1O18 R7 C15 r1-c2 r3-c3 ubiquinol--cytochrome-c reductase (EC 1.10.2.2) Rieske TC72021 AW037813 cLET3D18 XXIH9 T6O17 R8 C15 r3-c1 r2-c4 iron-sulfur protein-potato polyphenol oxidase precursor TC72054 AW650785 cLEI14K20 VIIC3 T2F5 R20 C6 r4-c2 r1-c3 polyphenol oxidase precursor TC72055 BG133913 cTOE14D12 XVIIIC4 T5E8 R17 C5 r3-c2 r4-c4 polyphenol oxidase precursor TC72056 AW217970 cTOD6A1 XVIF2 T4L4 R21 C12 r2-c2 r1-c4 polyphenoloxidase, P2 [Lycopersicon TC72057 BG129916 cTOF28D12 XXIH4 T6O7 R18 C15 r3-c1 r2-c4 esculentum = tomatoes, cv Tiny Tim LA154, flowers, Peptide Chloroplast, 587 aa]{circumflex over ( )}{circumflex over ( )}polyphenol oxidase precursor vacuolar ATP synthase subunit b isoform 1 subunit) TC72080 BE451002 cLEC16G9 XIVA1 T4A2 R23 C1 r2-c2 r1-c4 {Gossypium hirsutum}SP|Q43432|VAT1_GOSHI VACUOLA cytochrome p450 1xxvia2 {Solanum TC72085 AI779703 cLES8J16 XIA12 T3B23 R2 C2 r2-c1 r4-c3 melongena}SP|P37122|C762_SOLME CYTOCHROME P450 76A2 (EC 1.14.—.—) ethylene-responsive methionine synthase TC72099 AW649298 cLEI7F6 VIIF9 T2L17 R8 C12 r4-c2 r1-c3 cinnamic acid 4-hydroxylase {Capsicum annuum} TC72100 AW218565 cLEZ9N15 XIVA5 T4A10 R15 C1 r2-c2 r1-c4 cinnamic acid 4-hydroxylase {Capsicum chinense} TC72101 AI484136 cLER1C5 XA3 T3A6 R19 C1 r2-c1 r4-c3 glyceraldehyde 3-phosphate dehydrogenase b precursor, TC72118 BG128691 cTOF21D16 XIXE1 T5J1 R24 C10 r3-c2 r4-c4 chloroplast {Pisum sativum}SP|P12859|G3PB_PEA glyceraldehyde 3-phosphate dehydrogenase b precursor, TC72119 AI782763 cLES20B4 XXIH6 T6O11 R14 C15 r3-c1 r2-c4 chloroplast {Pisum sativum}SP|P12859|G3PB_PEA 4-hydroxyphenylpyruvate dioxygenase {Solenostemon TC72120 AI896928 cLEC24E23 IF6 T1K11 R14 C11 r1-c2 r3-c3 scutellarioides} 4-hydroxyphenylpyruvate dioxygenase {Solenostemon TC72121 BG126577 cTOF12B4 XVIIIH2 T5O4 R21 C15 r3-c2 r4-c4 scutellarioides} obtusifoliol 14-alpha-demethylase {Triticum TC72126 BG125458 cTOF8P9 XXIH12 T6O23 R2 C15 r3-c1 r2-c4 aestivum}SP|P93596|CP51_WHEAT CYTOCHROME P450 51 (EC 1. fructokinase 1 {Arabidopsis TC72131 BG139438 cLPP13M11 XVD8 T4H15 R12 C8 r2-c2 r1-c4 thaliana}GP|13878053|gb|AAK44104.1|AF370289_1|AF370289 putative fructok beta-glucosidase {Arabidopsis thaliana} TC72139 BG127001 cTOF14G15 XXIB1 T6C1 R24 C3 r3-c1 r2-c4 AP2 domain containing protein {Prunus armeniaca} TC72156 AW615838 cTOA17G2 XVID9 T4H18 R7 C8 r2-c2 r1-c4 leucine zipper-containing protein AT103 {Arabidopsis TC72159 AI776440 cLER18B9 IXH3 T3O5 R20 C15 r2-c1 r4-c3 thaliana}PIR|T47754|T47754 leucine zipper-cont proline oxidase precursor {Arabidopsis thaliana} TC72165 BG127967 cTOF18H21 XIXB12 T5D23 R2 C4 r3-c2 r4-c4 homeobox TC72179 BF050472 cLEM18A14 VA8 T2A15 R12 C1 r4-c2 r1-c3 cytosolic aconitase {Nicotiana tabacum} TC72186 BG135767 cTOE23F23 XVG12 T4N23 R2 C14 r2-c2 r1-c4 cytosolic aconitase {Nicotiana tabacum} TC72187 BG127318 cTOF16I5 XIXA9 T5B17 R8 C2 r3-c2 r4-c4 hypothetical Cys-3-His zinc finger protein {Arabidopsis TC72194 AW625359 cLEZ12O7 XIVD4 T4G8 R17 C7 r2-c2 r1-c4 thaliana}GP|6598933|gb|AAF18728.1|AC018721_(—) aminotransferase-like protein {Arabidopsis thaliana} TC72199 AW626087 cLEZ18C16 VB1 T2C1 R24 C3 r4-c2 r1-c3 PROBABLE VACUOLAR ATP SYNTHASE TC72206 AW223863 cLEN13L16 VIIIH8 T2P16 R9 C16 r4-c2 r1-c3 SUBUNIT D 2 (EC 3.6.1.34) (V-ATPASE D SUBUNIT 2) (VACUOLAR PROTON PUM malate dehydrogenase, glyoxysomal precursor TC72213 AI772692 cLER3F19 IB8 T1C15 R12 C3 r1-c2 r3-c3 {Citrullus vulgaris}EGAD|130842|139627 glyoxysomal mala w-3 desaturase {Solanum TC72222 AW616121 cLHT6C11 XVC9 T4F17 R8 C6 r2-c2 r1-c4 tuberosum}PIR|T07685|T07685 omega-3 fatty acid desaturase (EC 1.14.99.—)- ATP synthase gamma subunit, mitochondrial precursor TC72225 AI773341 cLER6A4 XC4 T3E8 R17 C5 r2-c1 r4-c3 {Ipomoea batatas}SP|P26360|ATP3_IPOBA ATP SYNTH nucleoside diphosphate kinase TC72228 BG130597 cTOF31F13 XXC4 T5F8 R17 C6 r3-c2 r4-c4 glutamine synthetase TC72235 BG129590 cTOF25C23 XIXG12 T5N23 R2 C14 r3-c2 r4-c4 sulfite reductase {Nicotiana TC72279 cLEC37G5 cLEC37G5 XXIF11 T6K21 R4 C11 r3-c1 r2-c4 tabacum}GP|3721540|dbj|BAA33531.1||D83583 Sulfite Reductase {Nicotiana ALTERNATIVE OXIDASE 1 PRECURSOR (EC 1.—.—.—).GP TC72280 BE449781 cLEY14I23 XIIIG7 T4M13 R12 C13 r2-c2 r1-c4 |558054|gb|AAC60576.1||S71335 alternative oxidase, A homologous to glucosyltransferases TC72286 BG123332 cTOF1J9 XIXD6 T5H11 R14 C8 r3-c2 r4-c4 CYTOCHROME P450 81E1 (EC 1.14.—.—) TC72288 AI778489 cLES5B19 XVB10 T4D19 R6 C4 r2-c2 r1-c4 (ISOFLAVONE 2′-HYDROXYLASE) (P450 91A4) (CYP GE-3).GP|2443348|db UDP-GLUCOSE 4-EPIMERASE (EC 5.1.3.2) TC72291 AW094482 cLET28L16 XIG6 T3N11 R14 C14 r2-c1 r4-c3 (GALACTOWALDENASE) (UDP-GALACTOSE 4- EPIMERASE).GP|8698725|gb| transaldolase TC72292 AW626005 cLEZ17N10 XIVE5 T4I10 R15 C9 r2-c2 r1-c4 transcription factor {Vicia TC72300 BG134485 cTOE16O12 XVIIH1 T5O1 R24 C15 r3-c2 r4-c4 faba}GP|2104681|emb|CAA66481.1||X97907 transcription factor {Vicia faba putative CONSTANS-like B-box zinc finger protein TC72313 BF113609 cLEY21L1 XIVB10 T4C20 R5 C3 r2-c2 r1-c4 {Arabidopsis thaliana}PIR|A84720|A84720 hypothetic glucose-6-phosphate 1-dehydrogenase {Solanum TC72317 BF113184 cLEG43F12 VIG2 T2M4 R21 C13 r4-c2 r1-c3 tuberosum}SP|P37830|G6PD_SOLTU GLUCOSE-6- PHOSPHATE 1-D glucose-6-phosphate 1-dehydrogenase {Solanum TC72318 AW223852 cLEN13J18 VIIIH6 T2P12 R13 C16 r4-c2 r1-c3 tuberosum}SP|P37830|G6PD_SOLTU GLUCOSE-6- PHOSPHATE 1-D pyruvate kinase-like protein {Arabidopsis TC72325 AW220370 cLEX10B10 XIIIA5 T4A9 R16 C1 r2-c2 r1-c4 thaliana}PIR|T47556|T47556 pyruvate kinase-like protein- beta-amylase {Prunus armeniaca} TC72330 AW223795 cLEN13N5 VIIIH9 T2P18 R7 C16 r4-c2 r1-c3 glucose-6-phosphate isomerase, cytosolic 1 (gpi) TC72335 AI779723 cLES8N20 XIB4 T3D7 R18 C4 r2-c1 r4-c3 (phosphoglucose isomerase) (pgi) (phosphohexose iso AP2 domain-containing transcription factor {Nicotiana TC72337 BG134369 cTOE16K11 XXIA7 T6A13 R12 C1 r3-c1 r2-c4 tabacum} pyruvate dehydrogenase E1 beta subunit isoform 1 {Zea TC72349 AW154894 cLEW1C3 XIIF1 T3L2 R23 C12 r2-c1 r4-c3 mays} fructose-1,6-bisphosphatase, cytosolic bisphosphate 1- TC72350 BF098452 cLEW27E8 XIIH5 T3P10 R15 C16 r2-c1 r4-c3 phosphohydrolase) (fbpase) (cy-f1) {Solanum tu fructose-1,6-bisphosphatase, cytosolic bisphosphate 1- TC72351 AW040771 cLET10L5 XIC5 T3F9 R16 C5 r2-c1 r4-c3 phosphohydrolase) (fbpase) (cy-f1) {Solanum tu isopentenyl diphosphate isomerase 1 {Nicotiana TC72352 BG129273 cTOF23H8 XXIG9 T6M17 R8 C13 r3-c1 r2-c4 tabacum} putative glucose regulated repressor protein TC72370 BG128772 cTOF22E10 XIXE10 T5J19 R6 C10 r3-c2 r4-c4 {Arabidopsis thaliana}PIR|A84649|A84649 probable gluco pyruvate dehydrogenase E1 alpha subunit {Arabidopsis TC72372 BE354897 cTOC14F12 XVIIC11 T5E21 R4 C5 r3-c2 r4-c4 thaliana} PYROPHOSPHATE-FRUCTOSE 6-PHOSPHATE 1- TC72375 BG125076 cTOF7H5 XXF10 T5L20 R5 C12 r3-c2 r4-c4 PHOSPHOTRANSFERASE BETA SUBUNIT (EC 2.7.1.90) (PFP) (6-PHOSPHO transketolase, chloroplast precursor {Solanum TC72376 AW398784 cLPT4F22 XVIA8 T4B16 R9 C2 r2-c2 r1-c4 tuberosum}SP|Q43848|TKTC_SOLTU TRANSKETOLASE, CHLOROP glutamyl-tRNA synthetase {Arabidopsis TC72377 AI781426 cLES15G16 XE3 T3I6 R19 C9 r2-c1 r4-c3 thaliana}PIR|T52043|T52043 probable glutamate- tRNA ligase (E URIDYLATE KINASE (EC 2.7.4.—) (UK) (URIDINE TC72400 BF114322 cLEY26B11 XIVC4 T4E8 R17 C5 r2-c2 r1-c4 MONOPHOSPHATE KINASE) (UMP KINASE) (UMP/CMP KINASE).GP| asparagine synthetase {Triphysaria TC72402 AW625684 cLEZ16B17 XIVD11 T4G22 R3 C7 r2-c2 r1-c4 versicolor}GP|2429282|gb|AAD05034.1||AF014056 asparagine synthet cytochrome p450 lxxii hydroxylase) (ge10h) TC72403 BE434310 cLEG16E11 VE10 T2I19 R6 C9 r4-c2 r1-c3 {Catharanthus roseus}SP|Q05047|CP72_CATRO CYTOCHROME P45 cytochrome P450 {Arabidopsis thaliana} TC72404 AI485298 cLED5C5 IVA11 T1B22 R3 C2 r1-c2 r3-c3 VACUOLAR ATP SYNTHASE SUBUNIT C (EC TC72410 BE451373 cLEY18A9 XIVA9 T4A18 R7 C1 r2-c2 r1-c4 3.6.1.34) (V-ATPASE C SUBUNIT) (VACUOLAR PROTON PUMP C SUBUNIT). phosphoenolpyruvate carboxylase 2 TC72426 BE458917 cLEM5A15 IVF8 T1L16 R9 C12 r1-c2 r3-c3 lipoxygenase{circumflex over ( )}{circumflex over ( )}loxc homologue TC72430 AW222576 cLEN8L9 IXD9 T3G17 R8 C7 r2-c1 r4-c3 lipoxygenase{circumflex over ( )}{circumflex over ( )}loxc homologue TC72431 AI778045 cLES3F16 XH3 T3O6 R19 C15 r2-c1 r4-c3 succinyl-CoA synthetase, alpha subunit {Arabidopsis TC72435 AW222820 cLEN9B13 IXD10 T3G19 R6 C7 r2-c1 r4-c3 thaliana} VACUOLAR ATP SYNTHASE SUBUNIT D (EC TC72437 AW929411 cTOC8F2 XVIIE12 T5I23 R2 C9 r3-c2 r4-c4 3.6.1.34) (V-ATPASE D SUBUNIT) (VACUOLAR PROTON PUMP D SUBUNIT). NADPH-cytochrome P450 oxidareductase (EC 1.—.—.—)- TC72444 AW441648 cLEN17N14 IVH4 T1P8 R17 C16 r1-c2 r3-c3 common tobacco ATP synthase beta subunit TC72461 AW617859 cLHT24H4 XXIA4 T6A7 R18 C1 r3-c1 r2-c4 putative sulfite oxidase {Arabidopsis TC72463 AW621692 cLEX13E13 XIIIC2 T4E3 R22 C5 r2-c2 r1-c4 thaliana}GP|6513940|gb|AAF14844.1|AC011664_26|AC011664 sulfit putative homeodomain transcription factor {Arabidopsis TC72471 AI488166 cLED21A22 IIIC3 T1F5 R20 C6 r1-c2 r3-c3 thaliana}PIR|F84565|F84565 probable homeodom NADP-dependent glyceraldehyde-3-phosphate TC72481 AW649868 cLEI9L22 VIIG7 T2N13 R12 C14 r4-c2 r1-c3 dehydrogenase (non-phosphorylating glyceraldehyde 3- phosph WRKY transcription factor Nt-SubD48 {Nicotiana TC72483 BF050338 cLEM17M14 VIIH2 T2P3 R22 C16 r4-c2 r1-c3 tabacum} putative anthocyanin 5-aromatic acyltransferase TC72484 AW096580 cLET39A17 XXIF5 T6K9 R16 C11 r3-c1 r2-c4 {Arabidopsis thaliana}PIR|G84823|G84823 probable an pyruvate dehydrogenase E1 beta subunit isoform 2 {Zea TC72498 AW222942 cLEN9N12 IXE3 T3I5 R20 C9 r2-c1 r4-c3 mays} S-adenosylmethionine decarboxylase {Nicotiana TC72506 BF051123 cLEM21L9 VF9 T2K17 R8 C11 r4-c2 r1-c3 tabacum}PIR|T01934|T01934 adenosylmethionine decarbox NADH-UBIQUINONE OXIDOREDUCTASE 24 KDA TC72512 AW622611 cLEX15D4 XIE4 T3J7 R18 C10 r2-c1 r4-c3 SUBUNIT PRECURSOR (EC 1.6.5.3) (EC 1.6.99.3).GP|7269018|emb|C phosphate/phosphoenolpyruvate translocator precursor TC72515 BG643700 cTOF32E22 XXC10 T5F20 R5 C6 r3-c2 r4-c4 {Nicotiana tabacum}GP|1778145|gb|AAB40648.1||U putative glucosyltransferase {Arabidopsis TC72520 AW625702 cLEZ16H1 XIVE1 T4I2 R23 C9 r2-c2 r1-c4 thaliana}PIR|H84870|H84870 probable glucosyltransferase [ pyruvate dehydrogenase TC72539 BG643832 cTOF33A1 XXC12 T5F24 R1 C6 r3-c2 r4-c4 zinc finger transcription factor-like protein {Arabidopsis TC72540 AW221733 cLEN3B6 XXH10 T5P20 R5 C16 r3-c2 r4-c4 thaliana}PIR|T49899|T49899 zinc finger t flavanone 3-hydroxylase-like protein {Arabidopsis TC72542 AI897731 cLED30B19 IIIE12 T1J23 R2 C10 r1-c2 r3-c3 thaliana} gamma-glutamylcysteine synthetase TC72560 BG125088 cTOF7J11 XXIC2 T6E3 R22 C5 r3-c1 r2-c4 transcription initiation factor iib (tfiib) {Glycine TC72566 BF050934 cLEM21C17 VIIIA1 T2B2 R23 C2 r4-c2 r1-c3 max}SP|P48513|TF2B_SOYBN TRANSCRIPTION INITIAT dihydroxy-acid dehydratase {Arabidopsis thaliana} TC72576 BG130088 cTOF29C14 XXA11 T5B22 R3 C2 r3-c2 r4-c4 arginine methyltransferase (paml) {Arabidopsis TC72613 AI781196 cLES14F12 XD11 T3G22 R3 C7 r2-c1 r4-c3 thaliana}GP|7269850|emb|CAB79709.1||AL161575 TC72613 AI781196 cLES14F12 XD11 T3G22 R3 C7 r2-c1 r4-c3 arginin N-hydroxycinnamoyl/benzoyltransferase {Ipomoea TC72632 AI898930 cLED36K11 IIIH2 T1P3 R22 C16 r1-c2 r3-c3 batatas} similar to ATPases associated with various cellular TC72650 BF051653 cLEM23D22 VIIIB9 T2D18 R7 C4 r4-c2 r1-c3 activites (Pfam: AAA.hmm, score: 230.91) {Arabid putative monosaccharide transporter 1 {Petunia x TC72655 BG138866 cLPP11G6 XVD3 T4H5 R20 C8 r2-c2 r1-c4 hybrida} 78 kDa glucose regulated protein homolog 5 precursor TC72660 AW622750 cTOB4O12 XVIIB3 T5C5 R20 C3 r3-c2 r4-c4 (grp 78-5) (immunoglobulin heavy subunit bindin threonine synthase {Solanum tuberosum} TC72666 AW651453 cLEI16P15 VIID3 T2H5 R20 C8 r4-c2 r1-c3 CONSTANS-like B-box zinc finger protein-like TC72668 BG129699 cTOF27L4 XXA6 T5B12 R13 C2 r3-c2 r4-c4 {Arabidopsis thaliana} Identical to ribose-phosphate pyrophosphokinase 2 TC72677 AW223107 cLEN10D3 VIIIG1 T2N2 R23 C14 r4-c2 r1-c3 (phosphoribosyl pyrophosphate synthetase 2) (PRSII NADH dehydrogenase {Solanum TC72678 BG643904 cTOF33O15 XXD3 T5H8 R17 C8 r3-c2 r4-c4 tuberosum}GP|668987|emb|CAA59063.1||X84320 NADH dehydrogenase {Solanum Similar to gb|Z84386 anthranilate N- TC72703 AW737648 cTOD3J14 XVIIG11 T5M21 R4 C13 r3-c2 r4-c4 hydroxycinnamoyl/benzoyltransferase from Dianthus caryophyllus. putative H+-transporting ATPase {Oryza sativa} TC72705 AW220712 cLEF2G23 IA12 T1A23 R2 C1 r1-c2 r3-c3 Similar to Populus balsamifera subsp. trichocarpa x TC72708 AI778197 cLES4A22 XH5 T3O10 R15 C15 r2-c1 r4-c3 Populus deltoides vegetative storage protein. (L cytochrome P450-dependent fatty acid hydroxylase TC72710 AW442394 cLEN22J6 VA9 T2A17 R8 C1 r4-c2 r1-c3 {Vicia sativa} anthocyanidin 3-O-glucosyltransferase {Petunia x TC72713 AW945115 cTOB13F3 IA2 T1A3 R22 C1 r1-c2 r3-c3 hybrida} cytochrome p450 lxxia4 {Solanum TC72718 AW223657 cLEN12N5 VIIIG12 T2N24 R1 C14 r4-c2 r1-c3 melongena}SP|P37117|C714_SOLME CYTOCHROME P450 71A4 (EC 1.14.—.—) ( cytochrome p450 lxxia4 {Solanum TC72719 BE353651 cTOA19J6 XVIE4 T4J8 R17 C10 r2-c2 r1-c4 melongena}SP|P37117|C714_SOLME CYTOCHROME P450 71A4 (EC 1.14.—.—) ( phosphoenolpyruvate carboxykinase {Flaveria pringlei} TC72722 AW030343 cLEC16F9 ID9 T1G17 R8 C7 r1-c2 r3-c3 phosphoribosyl pyrophosphate synthase {Spinacia TC72727 BG124244 cTOF4H7 XXE6 T5J12 R13 C10 r3-c2 r4-c4 oleracea} dehydroquinate dehydratase/shikimate:NADP TC72770 BE461692 cLEG39N19 VIE9 T2I18 R7 C9 r4-c2 r1-c3 oxidoreductase AP2 domain containing protein {Prunus armeniaca} TC72775 AW093577 cLET25E20 XIG2 T3N3 R22 C14 r2-c1 r4-c3 putative phosphate/phosphoenolpyruvate translocator TC72794 AW037415 cLET5A1 XXIE7 T6I13 R12 C9 r3-c1 r2-c4 {Arabidopsis thaliana} SNAP25A protein {Arabidopsis TC72817 BF051551 cLEM23I12 VIIIB10 T2D20 R5 C4 r4-c2 r1-c3 thaliana}GP|5731763|emb|CAB52582.1||X92419 SNPA25A protein {Arabidopsi heat shock transcription factor like protein {Arabidopsis TC72821 BF096782 cLEW17M17 IVF1 T1L2 R23 C12 r1-c2 r3-c3 thaliana}GP|2244754|emb|CAB1077.1||Z9733 ADP-glucose pyrophosphorylase large subunit 1 TC72843 AI781523 cLES16E9 XE9 T3I18 R7 C9 r2-c1 r4-c3 putative methylmalonate semi-aldehyde dehydrogenase TC72868 AW224041 cLEN14F7 IXA1 T3A1 R24 C1 r2-c1 r4-c3 {Arabidopsis thaliana}PIR|H84514|H84514 hypothe flavonol 3-o-glucosyltransferase 6 {Manihot TC72874 AW036019 cLEC21A15 IE7 T1I13 R12 C9 r1-c2 r3-c3 esculenta}SP|Q40288|UFO6_MANES FLAVONOL 3- O-GLUCOSYLTRA Identical to gene ZW10 from Arabidopsis thaliana TC72889 BG127811 cTOF18M15 XXIIA6 T6A12 R13 C1 r3-c1 r2-c4 gb|AB028195 and is a member of the Phosphoglycerate coproporphyrinogen iii oxidase precursor TC72896 AW931818 cTOF4P23 IVH2 T1P4 R21 C16 r1-c2 r3-c3 (coproporphyrinogenase) (coprogen oxidase) {Nicotiana tabac zinc finger protein-like {Arabidopsis TC72898 AI486585 cLED6E7 IVB8 T1D16 R9 C4 r1-c2 r3-c3 thaliana}GP|5006473|gb|AAD37511.1|AF139098_1|AF139098 putativ caffeoyl-CoA O-methyltransferase {Nicotiana TC72904 AI895091 cLEC6D10 XIIF2 T3L4 R21 C12 r2-c1 r4-c3 tabacum}GP|1103487|emb|CAA91228.1||Z56282 caffeoyl-CoA phosphoglycerate mutase {Solanum tuberosum} TC72922 AW648487 cLEI4B6 XIIF7 T3L14 R11 C12 r2-c1 r4-c3 acetyl-CoA C-acetyltransferase {Arabidopsis thaliana} TC72945 AW928977 cTOC4K4 XVIID11 T5G21 R4 C7 r3-c2 r4-c4 acetyl-CoA C-acetyltransferase {Arabidopsis thaliana} TC72946 AW398370 cLPT6I1 XVIB10 T4D20 R5 C4 r2-c2 r1-c4 putative NADH-ubiquinone oxireductase {Arabidopsis TC72951 AW621179 cLEX11E19 XIIIB2 T4C3 R22 C3 r2-c2 r1-c4 thaliana}PIR|C84588|C84588 probable NADH-ubiquin acetyl-CoA C-acetyltransferase {Arabidopsis thaliana} TC72956 AW621890 cLEX13L9 XXIF6 T6K11 R14 C11 r3-c1 r2-c4 malonyl-CoA: ACP transacylase {Perilla frutescens} TC72961 BE450922 cLEY15N21 XIIIH8 T4O15 R12 C15 r2-c2 r1-c4 N-carbamyl-L-amino acid amidohydrolase-like protein TC72977 AW442132 cLEN21O18 IXC3 T3E5 R20 C5 r2-c1 r4-c3 {Axabidopsis thaliana} uracil phosphoribosyltransferase {Nicotiana TC72985 BG124328 cTOF4N12 XXE7 T5J14 R11 C10 r3-c2 r4-c4 tabacum}SP|P93394|UPP_TOBAC URACIL PHOSPHORIBOSYLTRANSF heat stress transcription factor A3 {Lycopersicon TC72992 BG642641 cTOF25C4 XIXH1 T5P1 R24 C16 r3-c2 r4-c4 peruvianum} invertase-like protein {Arabidopsis TC73000 AI485121 cLED7B14 VC7 T2E13 R12 C5 r4-c2 r1-c3 thaliana}GP|7270437|emb|CAB80203.1||AL161586 invertase-like pro contains similarity to acyl-CoA TC73001 BE459589 cLEM7B1 VIIE9 T2J17 R8 C10 r4-c2 r1-c3 thioesterase~gene_id: K23F3.9 {Arabidopsis thaliana} acetylornithine aminotransferase precursor {Alnus TC73014 AI490283 cLED24N6 IIID1 T1H1 R24 C8 r1-c2 r3-c3 glutinosa}SP|O04866|ARGD_ALNGL ACETYLORNITHINE AM glucose-6-phosphate isomerase {Spinacia TC73016 AW399786 cLPT10F14 VC2 T2E3 R22 C5 r4-c2 r1-c3 oleracea}PIR|T09153|T09153 glucose-6-phosphate isomerase (E hydroxypyruvate reductase {Bruguiera gymnorhiza} TC73027 AI487051 cLED9G3 IVC12 T1F24 R1 C6 r1-c2 r3-c3 PROTEIN-L-ISOASPARTATE O- TC73037 AI776861 cLER20E3 XB1 T3C2 R23 C3 r2-c1 r4-c3 METHYLTRANSFERASE (EC 2.1.1.77) (PROTEIN- BETA-ASPARTATE METHYLTRANSFERASE) putative anthocyanidin-3-glucoside TC73055 BG123229 cTOF1C4 XIXC12 T5F23 R2 C6 r3-c2 r4-c4 rhamnosyltransferase {Arabidopsis thaliana}PIR|D84614|D84614 hyp putative RING-H2 zinc finger protein ATL6 TC73059 AW399786 cLEG24D12 VB2 T2C3 R22 C3 r4-c2 r1-c3 {Arabidopsis thaliana} adenosine kinase {Arabidopsis TC73160 BE462073 cTOA11E17 XXIG5 T6M9 R16 C13 r3-c1 r2-c4 thaliana}GP|7378610|emb|CAB83286.1||AL162751 adenosine kinase-like pr putative PHD-type zinc finger protein {Arabidopsis TC73164 BF051010 cLEM21E20 XXIB6 T6C11 R14 C3 r3-c1 r2-c4 thaliana}PIR|A84437|A84437 probable PHD-type zin quinolinate phosphoribosyltransferase {Nicotiana TC73169 BG130955 cTOE2C9 XVIF8 T4L16 R9 C12 r2-c2 r1-c4 tabacum} 5-enolpyruvylshikimate-3-phosphate synthase precursor TC73179 BG126520 cTOF12F23 XVIIIH3 T5O6 R19 C15 r3-c2 r4-c4 (EC 2.5.1.19) transcription factor TC73183 AW218738 cLEX1C5 XIIID5 T4G9 R16 C7 r2-c2 r1-c4 Dof zinc finger protein {Arabidopsis TC73204 AI771243 cLED28N11 IIIE4 T1J7 R18 C10 r1-c2 r3-c3 thaliana}GP|9280230|dbj|BAB01720.1||AB023045 Dof zinc finger p aldose 1-epimerase-like protein {Arabidopsis TC73210 BE461978 cLEG40O8 VIF1 T2K2 R23 C11 r4-c2 r1-c3 thaliana}PIR|T07719|T07719 aldose 1-epimerase homolog glucosyl transferase {Nicotiana TC73225 AI483731 cLED23J21 XXID2 T6G3 R22 C7 r3-c1 r2-c4 tabacum}GP|1805359|dbj|BAA19155.1||AB000623 glucosyl transferase {N unnamed protein product TC73255 AW615991 cTOA17D2 XVID8 T4H16 R9 C8 r2-c2 r1-c4 {unidentified}□GP|2462931|emb|CAB06082.1||Z83833 UDP-glucose: sterol glucosyl homogentisate 1,2-dioxygenase TC73262 AW092200 cLET17L20 XID10 T3H19 R6 C8 r2-c1 r4-c3 putative aspartate aminotransferase; 38163-36256 TC73280 BG133934 cTOE14H6 XVIIIC6 T5E12 R13 C5 r3-c2 r4-c4 {Arabidopsis thaliana}PIR|C96835|C96835 hypothetic ATP synthase alpha chain {Vigna radiata} TC73289 AW031503 cLEC40G14 IID5 T1G10 R15 C7 r1-c2 r3-c3 MYB-like DNA-binding protein {Catharanthus roseus} TC73317 BG128786 cTOF22G14 XIXE12 T5J23 R2 C10 r3-c2 r4-c4 CYTOCHROME P450 90A1 (EC 1.14.—.—). TC73326 BE449595 cLHT32I3 XVC8 T4F15 R12 C6 r2-c2 r1-c4 GP|853719|emb|CAA60793.1||X87367 CYP90 protein {Arabidopsis thal vsf-1{circumflex over ( )}{circumflex over ( )}transcription factor VSF-1 TC73332 AW094595 cLET29E6 XIG9 T3N17 R8 C14 r2-c1 r4-c3 ATP synthase alpha subunit {Nicotiana TC73341 BF112918 cLEG43G11 VIG3 T2M6 R19 C13 r4-c2 r1-c3 tabacum}SP|P00823|ATPA_TOBAC ATP SYNTHASE ALPHA CHAIN (EC 3.6 isoflavone reductase homolog {Solanum TC73357 BG125717 cTOF9H3 XXG9 T5N18 R7 C14 r3-c2 r4-c4 tuberosum}SP|P52578|IFRH_SOLTU ISOFLAVONE REDUCTASE HOMOLOG ( fumarase {Solanum TC73367 BF112535 cLEG41L11 VC9 T2E17 R8 C5 r4-c2 r1-c3 tuberosum}GP|1488652|emb|CAA62817.1||X91615 fumarase {Solanum tuberosum}PIR|T073 ornithine carbamoyltransferase; OCTase {Canavalia TC73370 AI486970 cLED6P9 IVC2 T1F4 R21 C6 r1-c2 r3-c3 lineata}GP|12003188|gb|AAG43481.1|AF203688_1|AF20 N-glyceraldehyde-2-phosphotransferase-like TC73374 BG630730 cLEL4E1 XXIG4 T6M7 R18 C13 r3-c1 r2-c4 {Arabidopsis thaliana} putative cinnamyl alcohol dehydrogenase {Malus x TC73375 BE451381 cLEY18C9 XIVA10 T4A20 R5 C1 r2-c2 r1-c4 domestica}PIR|T16995|T16995 probable cinnamyl-alco putative anthocyanidin-3-glucoside TC73422 AW441205 cLEN4F1 IXC10 T3E19 R6 C5 r2-c1 r4-c3 rhamnosyltransferase {Arabidopsis thaliana}PIR|D84614|D84614 hyp serine/threonine-specific protein kinase NAK TC73426 AI772369 cLER2B1 XXIA11 T6A21 R4 C1 r3-c1 r2-c4 {Arabidopsis thaliana}PIR|T48250|T48250 serine/threoni putative threonine dehydratase/deaminase {Oryza TC73457 BE449339 cLPT23P6 XVB11 T4D21 R4 C4 r2-c2 r1-c4 sativa} pyruvate dehydrogenase kinase {Arabidopsis thaliana} TC73458 BE459347 cLEM6D21 IVH6 T1P12 R13 C16 r1-c2 r3-c3 Cytochrome P450-like protein {Arabidopsis TC73461 AW929893 cTOC8A14 IVE10 T1J20 R5 C10 r1-c2 r3-c3 thaliana}GP|7270098|emb|CAB79912.1||AL161580 Cytochrome P putative arginine methyltransferase {Arabidopsis TC73476 AI899735 cLES20J21 IA9 T1A17 R8 C1 r1-c2 r3-c3 thaliana} glutamine synthetase {Nicotiana TC73479 AW621882 cLEX13J15 XIIIC3 T4E5 R20 C5 r2-c2 r1-c4 tabacum}GP|1419094|emb|CAA65173.1||X95932 glutamine synthetase {Nic glucosyl transferase {Nicotiana TC73487 AI896066 cLEC13B18 IC8 T1E15 R12 C5 r1-c2 r3-c3 tabacum}GP|1805359|dbj|BAA19155.1||AB000623 glucosyl transferase {N putative RING zinc finger protein; 36546-35989 TC73490 AW223952 cLEN14A6 VIIIH11 T2P22 R3 C16 r4-c2 r1-c3 {Arabidopsis thaliana}GP|12323975|gb|AAG51946.1|AC01 cytochrome P450 {Nicotiana tabacum} TC73493 AW616568 cLHT11B6 XIVH2 T4O4 R21 C15 r2-c2 r1-c4 PHOSPHOGLUCOMUTASE, CYTOPLASMIC (EC TC73495 BG132150 cTOE6J5 XVIIC1 T5E1 R24 C5 r3-c2 r4-c4 5.4.2.2) (GLUCOSE PHOSPHOMUTASE) (PGM).GP|8250624|emb|CAB93681. starch phosphorylase (AA 1-966) {Solanum tuberosum} TC73506 AW738720 cTOD8G8 XVIIIB3 T5C6 R19 C3 r3-c2 r4-c4 alpha-glucan phosphorylase, 1 isozyme 1 precursor TC73507 BG642630 cTOF25A4 XIXG10 T5N19 R6 C14 r3-c2 r4-c4 (starch phosphorylase 1-1) {Solanum tuberosum}SP| acetyl-coA dehydrogenase, putative {Arabidopsis TC73523 BG127274 cTOF14P14 XVIIF10 T5K19 R6 C11 r3-c2 r4-c4 thaliana} 1-asparaginase (1-asparagine amidohydrolase) TC73526 BG123680 cTOF2D8 XXB6 T5D12 R13 C4 r3-c2 r4-c4 {Arabidopsis thaliana} PROBABLE TC73527 AW622713 cTOB4I2 XVIIB2 T5C3 R22 C3 r3-c2 r4-c4 PHOSPHORIBOSYLFORMYLGLYCINAMIDINE SYNTHASE, CHLOROPLAST PRECURSOR (EC 6.3.5.3) (FGAM SYNTHA Putative phospholipid cytidylyltransferase {Oryza TC73548 BF096825 cLEW17K4 XIID10 T3H20 R5 C8 r2-c1 r4-c3 sativa} 2-oxoglutarate/malate translocator {Arabidopsis TC73585 BG643918 cTOF33D5 XXD1 T5H2 R23 C8 r3-c2 r4-c4 thaliana} putative ripening-related bZIP protein {Vitis vinifera} TC73588 AW222150 cLEN7I11 XIIIA2 T4A3 R22 C1 r2-c2 r1-c4 ethylene-responsive transcriptional coactivator TC73593 AW031517 cLEC40C16 IID4 T1G8 R17 C7 r1-c2 r3-c3 PHOSPHOGLUCOMUTASE, CYTOPLASMIC (EC TC73595 BE458969 cLEM5K5 XXIG11 T6M21 R4 C13 r3-c1 r2-c4 5.4.2.2) (GLUCOSE PHOSPHOMUTASE) (PGM).GP|8250624|emb|CAB93681. putative transcripton factor {Nostoc sp. PCC 7120} TC73599 AW945043 cTOB12P12 XVIH3 T4P6 R19 C16 r2-c2 r1-c4 microsomal oleate desaturase {Arachis ipaensis} TC73604 AI775627 cLER16G21 XXIC3 T6E5 R20 C5 r3-c1 r2-c4 pyruvate dehydrogenase e1 component, alpha subunit TC73607 AI782695 cLES20G10 XG6 T3M12 R13 C13 r2-c1 r4-c3 precursor {Solanum tuberosum}SP|P52903|ODPA_SOLT enoyl-ACP reductase {Nicotiana TC73615 AW399701 cLPT8B18 IVD10 T1H20 R5 C8 r1-c2 r3-c3 tabacum}GP|2204236|emb|CAA74176.1||Y13861 enoyl-ACP reductase {Nicot putative dehydroquinase shikimate dehydrogenase TC73630 BF096277 cLEW11I15 XIID7 T3H14 R11 C8 r2-c1 r4-c3 {Arabidopsis thaliana} myb-related transcription factor {Lycopersicon TC73643 AI487918 cLED10D18 XXIF1 T6K1 R24 C11 r3-c1 r2-c4 esculentum}PIR|T07393|T07393 myb-related transcripti bZIP transcriptional activator RSG, putative TC73646 AW616861 cLHT17P21 XIIID4 T4G7 R18 C7 r2-c2 r1-c4 {Arabidopsis thaliana}GP|12321383|gb|AAG50761.1|AC0791 putative zinc finger protein {Oryza sativa} TC73652 AI897679 cLED30G19 IIIF2 T1L3 R22 C12 r1-c2 r3-c3 pyruvate kinase (EC 2.7.1.40) A, chloroplast-common TC73662 AW625105 cLEZ10G1 XIVC11 T4E22 R3 C5 r2-c2 r1-c4 tobacco 6-phosphogluconate dehydrogenase, putative; 13029-14489 TC73678 AW624047 cTOB13N24 XVIH10 T4P20 R5 C16 r2-c2 r1-c4 {Arabidopsis thaliana} zinc-finger protein, putative; 7043-7771 {Arabidopsis TC73679 BF050885 cLEM19J4 VIIIC3 T2F6 R19 C6 r4-c2 r1-c3 thaliana}PIR|H86450|H86450 probable zinc-fing ornithine aminotransferase {Arabidopsis thaliana} TC73702 AW222058 cLEN6D8 IXC12 T3E23 R2 C5 r2-c1 r4-c3 pyrophosphate-dependent phosphofructo-1-kinase TC73706 BE433184 cLEG12J15 XIIB5 T3D10 R15 C4 r2-c1 r4-c3 {Arabidopsis thaliana}GP|7269478|emb|CAB79482.1||AL1 sugar-phosphate isomerase-like protein {Arabidopsis TC73722 BE451590 cLEY19P11 XIVB3 T4C6 R19 C3 r2-c2 r1-c4 thaliana}PIR|T47628|T47628 sugar-phosphate isom cytochrome P450, putative {Arabidopsis thaliana} TC73737 BE463315 cTOC12H5 XVIIC6 T5E11 R14 C5 r3-c2 r4-c4 RING-H2 finger protein RHF2a {Arabidopsis TC73753 AW617482 cLHT23O11 XIIIA3 T4A5 R20 C1 r2-c2 r1-c4 thaliana}GP|13374859|emb|CAC34493.1||AL589883 RING-H2 fin Contains similarity to gb|AF136530 transcriptional TC73763 AW980011 cLEC19M9 XIIF10 T3L20 R5 C12 r2-c1 r4-c3 regulator from Zea mays. {Arabidopsis thaliana}P glucose-6-phosphate 1-dehydrogenase {Solanum TC73842 BE451514 cLEY19C18 XIVA12 T4A24 R1 C1 r2-c2 r1-c4 tuberosum} putative pyrophosphate-fructose-6-phosphate 1- TC73845 AW033973 cLEC38A6 IIC6 T1E12 R13 C5 r1-c2 r3-c3 phosphotransferase {Arabidopsis thaliana}PIR|B84613| putative glucosyltransferase {Arabidopsis TC73904 AW035536 cLEC39G15 IB10 T1C19 R6 C3 r1-c2 r3-c3 thaliana}PIR|E84680|E84680 probable glucosyltransferase [ acetyl-CoA synthetase {Solanum tuberosum} TC73927 BG130097 cTOF29E8 XXA12 T5B24 R1 C2 r3-c2 r4-c4 Knotted 1 (TKn1) TC73929 AW648828 cLEI6C19 IB11 T1C21 R4 C3 r1-c2 r3-c3 homeotic protein BEL1 homolog {Arabidopsis thaliana} TC73945 AI780410 cLES11N9 XD6 T3G12 R13 C7 r2-c1 r4-c3 flavanone 3-hydroxylase-like protein {Arabidopsis TC73949 BE450984 cLEY16C7 XIIIH12 T4O23 R2 C15 r2-c2 r1-c4 thaliana} putative cinnamoyl CoA reductase {Arabidopsis TC73957 AW616521 cLHT11H15 XIVH5 T4O10 R15 C15 r2-c2 r1-c4 thaliana}PIR|C84630|C84630 probable cinnamoyl CoA red glucosyl transferase {Nicotiana TC73986 BE434399 cLEG16L10 VF2 T2K3 R22 C11 r4-c2 r1-c3 tabacum}GP|1805359|dbj|BAA19155.1||AB000623 glucosyl transferase {N helicase-like transcription factor-like protein TC73997 BG124688 cTOF6I11 XXF2 T5L4 R21 C12 r3-c2 r4-c4 {Arabidopsis thaliana} pyruvate dehydrogenase E1 beta subunit isoform 1 {Zea TC74002 AI771828 cLED38G13 IIIH7 T1P13 R12 C16 r1-c2 r3-c3 mays} fructose-6-phosphate 2-kinase/fructose-2,6- TC74004 BF112964 cLEG43O19 VIG7 T2M14 R11 C13 r4-c2 r1-c3 bisphosphatase {Solanum tuberosum}PIR|T07016|T07016 6-ph 1,4-alpha-glucan branching enzyme {Solanum TC74010 AW929962 cLEF40A9 IVE9 T1J18 R7 C10 r1-c2 r3-c3 tuberosum}□GP|1621012|emb|CAA70038.1||Y08786 1,4-alpha-gl 76 kDa mitochondrial complex I subunit {Solanum TC74019 BG124963 cTOF7O21 XXG2 T5N4 R21 C14 r3-c2 r4-c4 tuberosum}SP|Q43644|NUAM_SOLTU NADH- UBIQUINONE OXID Similar to ATP-citrate-lyase {Arabidopsis TC74060 BF050945 cLEM21G15 XXID9 T6G17 R8 C7 r3-c1 r2-c4 thaliana}PIR|F96633|F96633 hypothetical protein F8A5.32 [ putative anthocyanidin-3-glucoside TC74086 AW647635 cLEI10B9 VIIA8 T2B15 R12 C2 r4-c2 r1-c3 rhamnosyltransferase {Arabidopsis thaliana}PIR|D84614|D84614 hyp floral homeotic protein pmads 2 {Petunia TC74087 BG627196 cLEL16I15 XXIC4 T6E7 R18 C5 r3-c1 r2-c4 hybrida}SP|Q07474|MAD2_PETHY FLORAL HOMEOTIC PROTEIN PMADS CYTOCHROME P450 71D10 (EC 1.14.—.—). TC74103 AW218370 cLEZ7L22 XIVB2 T4C4 R21 C3 r2-c2 r1-c4 GP|2739000|gb|AAB94588.1||AF022459 CYP71D10p {Glycine max}PIR| putative CONSTANS-like B-box zinc finger protein TC74105 BG129734 cTOF28C7 XXA8 T5B16 R9 C2 r3-c2 r4-c4 {Arabidopsis thaliana}PIR|G84920|G84920 hypothetic Similar to gb|X90982 phosphoenolpyruvate carboxylase TC74116 AI490644 cLED24K5 VIIIC12 T2F24 R1 C6 r4-c2 r1-c3 (ppcl) from Solanum tuberosum. {Arabidopsis tha putative lipoxygenase {Arabidopsis TC74124 BE353443 cTOA19O11 VA11 T2A21 R4 C1 r4-c2 r1-c3 thaliana}PIR|B96699|B96699 probable lipoxygenase F12B7.11 [impor putative beta-amylase {Arabidopsis TC74131 BG642863 cTOF25L12 XIXH2 T5P3 R22 C16 r3-c2 r4-c4 thaliana}GP|5302810|emb|CAB46051.1||Z97342 putative beta-amylase UDP-glucose:protein transglucosylase {Solanum TC74136 BE353792 cTOD6G2 VA3 T2A5 R20 C1 r4-c2 r1-c3 tuberosum} hydroxymethyltransferase {Arabidopsis TC74141 BE449811 cLEY14O19 XIIIG11 T4M21 R4 C13 r2-c2 r1-c4 thaliana}GP|2244749|emb|CAB10172.1||Z97335 hydroxymethyltrans hexose transporter {Nicotiana tabacum} TC74146 BG642646 cTOF25C18 XIXG11 T5N21 R4 C14 r3-c2 r4-c4 alpha-glucosidase {Solanum tuberosum subsp. TC74149 BE437180 cLEG35B16 XVIA11 T4B22 R3 C2 r2-c2 r1-c4 tuberosum} ATP synthase delta' subunit, mitochondrial precursor TC74166 BF176603 cLEZ20N15 XIVG3 T4M6 R19 C13 r2-c2 r1-c4 {Ipomoea batatas}SP|Q40089|ATP4_IPOBA ATP SYNT knotted1-like homeobox protein {Malus TC74178 BG127568 cTOF17B16 XIXA11 T5B21 R4 C2 r3-c2 r4-c4 domestica}SP|O04136|HKL3_MALDO HOMEOBOX PROTEIN KNOTTED-1 LIK GLYCINE DEHYDROGENASE TC74186 BG139081 cLPP12A23 XVD5 T4H9 R16 C8 r2-c2 r1-c4 [DECARBOXYLATING], MITOCHONDRIAL PRECURSOR (EC 1.4.4.2) (GLYCINE DECARBOXYLASE contains similarity to CONSTANS TC74187 AW037464 cLET4F4 XIIF4 T3L8 R17 C12 r2-c1 r4-c3 homologs~gene_id: MIF21.14 {Arabidopsis thaliana} chalcone synthase TC74227 BG628623 cLEL22P8 XXIF4 T6K7 R18 C11 r3-c1 r2-c4 ADP-glucose pyrophosphorylase large subunit TC74234 AI776884 cLER20I1 XB2 T3C4 R21 C3 r2-c1 r4-c3 aldose 1-epimerase-like protein {Arabidopsis thaliana} TC74239 AW223542 cLEN12C22 VIIIG8 T2N16 R9 C14 r4-c2 r1-c3 3-phosphoshikimate 1-carboxyvinyltransferase TC74249 AI780056 cLES10E5 XC12 T3E24 R1 C5 r2-c1 r4-c3 precursor (5-enolpyruvylshikimate-3-phosphate synthase) CYTOCHROME P450 98A2 (EC 1.14.—.—). TC74259 BE451618 cLEY20I21 XIVB4 T4C8 R17 C3 r2-c2 r1-c4 GP|2738998|gb|AAB94587.1||AF022458 CYP98A2p {Glycine max}PIR|T0 zinc finger protein {Oryza sativa}PIR|JE0113|JE0113 TC74290 AI777848 cLES3A24 XH1 T3O2 R23 C15 r2-c1 r4-c3 zinc-finger protein S3574 [imported]-rice Chain A, Glycolate Oxidase (E.C.1.1.3.15) Mutant With TC74300 AW441496 cLEN17M12 IXB1 T3C1 R24 C3 r2-c1 r4-c3 Tyr 24 Replaced By Phe (Y24f)GP|999543|pdb|1G RING finger-like protein {Arabidopsis TC74308 AW220427 cLEX10L12 XIIIA8 T4A15 R12 C1 r2-c2 r1-c4 thaliana}PIR|T47605|T47605 RING finger-like protein- Arabido Contains similarity to acyl-CoA thioesterase from TC74331 BG629827 cLEL30C6 XXIE1 T6I1 R24 C9 r3-c1 r2-c4 Streptomyces coelicolor A3(2) gb|AL163641. EST gb putative bZIP transcription factor {Arabidopsis TC74347 BG644072 cTOF34C15 XXD5 T5H10 R15 C8 r3-c2 r4-c4 thaliana}PIR|G84831|G84831 probable bZIP transcript hyoscyamine 6-dioxygenase hydroxylase, putative TC74351 AW033695 cLEC29O19 IH2 T1O3 R22 C15 r1-c2 r3-c3 {Arabidopsis thaliana}PIR|G86472|G86472 probable hy leucine zipper transcription factor TGA2.1 {Nicotiana TC74356 BG129128 cTOF23K20 XIXG1 T5N1 R24 C14 r3-c2 r4-c4 tabacum}SP|O24160|TG21_TOBAC TGACG- SEQUENCE S succinate dehydrogenase flavoprotein alpha subunit TC74365 AW398787 cLPT4H10 XVIA9 T4B18 R7 C2 r2-c2 r1-c4 {Arabidopsis thaliana}GP|8843734|dbj|BAA97282.1| cytochrome P450 {Arabidopsis thaliana} TC74397 AW617140 cLHT21D12 XVB8 T4D15 R12 C4 r2-c2 r1-c4 N-hydroxycinnamoyl/benzoyltransferase-like protein TC74426 AW617365 cLHT22D16 XVB1 T4D1 R24 C4 r2-c2 r1-c4 {Arabidopsis thaliana} phosphoribosyl pyrophosphate synthase isozyme 4 TC74427 AI485769 cLED4K18 IVA6 T1B12 R13 C2 r1-c2 r3-c3 {Spinacia oleracea} (+)-DELTA-CADINENE SYNTHASE ISOZYME A TC74429 AW035405 cLEC38O24 IIC10 T1E20 R5 C5 r1-c2 r3-c3 (EC 4.6.1.11) (D-CADINENE SYNTHASE).GP|1217956|emb|CAA65289.1 contains similarity to apoptosis antagonizing TC74441 AW036113 cLEE1M7 IVD8 T1H16 R9 C8 r1-c2 r3-c3 transcription factor~gene_id: MFB13.10 {Arabidopsis tha putative sugar transporter; member of major facilitative TC74458 AI777293 cLER20L10 XB4 T3C8 R17 C3 r2-c1 r4-c3 superfamily; integral membrane protein {Bet 4-alpha-glucanotransferase precursor TC74463 AW737543 cTOD3F15 XVIIG8 T5M15 R12 C13 r3-c2 r4-c4 (disproportionating enzyme) (d-enzyme) {Solanum tuberosum}SP|Q NADH glutamate dehydrogenase {Nicotiana TC74481 AW930356 cLEF43J5 XXIIA9 T6A18 R7 C1 r3-c1 r2-c4 plumbaginifolia}SP|O04937|DHEA_NICPL GLUTAMATE DEHYDROGENAS bZIP protein {Arabidopsis thaliana}PIR|T49227|T49227 TC74487 AW216659 cLET39D19 IIF9 T1K18 R7 C11 r1-c2 r3-c3 bZIP protein-Arabidopsis thaliana zinc-finger protein, putative; 7043-7771 {Arabidopsis TC74525 BG643132 cTOF26N17 XIXH11 T5P21 R4 C16 r3-c2 r4-c4 thaliana}PIR|H86450|H86450 probable zinc-fing cytochrome P450 {Helianthus tuberosus} TC74527 AI776121 cLER17B3 IXG12 T3M23 R2 C13 r2-c1 r4-c3 fructose-bisphosphate aldolase, cytoplasmic isozyme 1 TC74553 AW929679 cTOC10G23 XVIIC3 T5E5 R20 C5 r3-c2 r4-c4 {Pisum sativum}SP|P46256|ALF1_PEA FRUCTOSE- BI transcriptional adaptor ADA2b {Arabidopsis thaliana} TC74560 BE459241 cLEM5P22 IVH7 T1P14 R11 C16 r1-c2 r3-c3 putative oxalyl-CoA decarboxylase {Oryza sativa} TC74622 AW094043 cLET27G5 XXIE11 T6I21 R4 C9 r3-c1 r2-c4 putative UDP-N-acetylglucosamine--N-acetylmuramyl- TC74633 BF051710 cLEM24A9 VIIIB12 T2D24 R1 C4 r4-c2 r1-c3 (pentapeptide)-pyrophosphoryl-undecaprenol N-acety G-Box binding protein 2 {Catharanthus roseus} TC74645 BG643085 cTOF26F11 XIXH5 T5P9 R16 C16 r3-c2 r4-c4 putative indole-3-glycerol phosphate synthase TC74653 AW648549 cLEI4P2 VIIE8 T2J15 R12 C10 r4-c2 r1-c3 {Arabidopsis thaliana}PIR|B84457|B84457 probable indo contains similarity to nucleotide sugar epimerases TC74661 BG126144 cTOF11K17 XVIIIG12 T5M24 R1 C13 r3-c2 r4-c4 {Arabidopsis thaliana}GP|7267098|emb|CAB80769.1| contains similarity to ATPases associated with various TC74673 BG123268 cTOF1K10 XIXD7 T5H13 R12 C8 r3-c2 r4-c4 cellular activities (Pfam: AAA.hmm, score: 15 putative dihydrolipoamide succinyltransferase TC74697 BE353150 cLEZ17N3 XIVE6 T4I12 R13 C9 r2-c2 r1-c4 {Arabidopsis thaliana}GP|7269544|emb|CAB79546.1||AL16 auxin-induced basic helix-loop-helix transcription TC74751 AW650619 cLEI13H3 VIIB10 T2D19 R6 C4 r4-c2 r1-c3 factor, putative {Arabidopsis thaliana}GP|123213 Myb-related transcription factor-like protein TC74758 BF097751 cLEW23B13 XIIG2 T3N4 R21 C14 r2-c1 r4-c3 {Arabidopsis thaliana} contains similarity to enolase- TC74779 AW034046 cLEC37M7 IIC5 T1E10 R15 C5 r1-c2 r3-c3 phosphatase~gene_id: K19P17.1 {Arabidopsis thaliana} formyl transferase, putative {Arabidopsis TC74804 BG132111 cTOE6O24 XVIIG2 T5M3 R22 C13 r3-c2 r4-c4 thaliana}PIR|H96690|H96690 probable formyl transferase F2 immediate-early salicylate-induced glucosyltransferase TC74808 AW624795 cLEZ8O11 XIVG8 T4M16 R9 C13 r2-c2 r1-c4 {Nicotiana tabacum}GP|1685005|gb|AAB36653.1| putative para-aminobenzoate synthase and glutamine TC74821 AW223881 cLEN13P22 VIIIH10 T2P20 R5 C16 r4-c2 r1-c3 amidotransferase, a bifunctional enzyme {Arabidop alpha-glucosidase {Solanum tuberosum subsp. TC74846 AI775531 cLER15F22 IXF8 T3K15 R12 C11 r2-c1 r4-c3 tuberosum} MADS-box transcription factor FBP4 {Petunia x TC74865 AW441864 cLEN18D10 IXB6 T3C11 R14 C3 r2-c1 r4-c3 hybrida} NAD-dependent isocitrate dehydrogenase {Nicotiana TC74889 BG123588 cTOF2M10 XXB9 T5D18 R7 C4 r3-c2 r4-c4 tabacum} cytochrome p450 lxxviia1 {Solanum TC74928 AW092327 cLET19H11 XIE1 T3J1 R24 C10 r2-c1 r4-c3 melongena}SP|P37123|C771_SOLME CYTOCHROME P450 77A1 (EC 1.14.—.—) threonine deaminase {Nicotiana attenuata} TC74935 AW934272 cLEF58K10 VC10 T2E19 R6 C5 r4-c2 r1-c3 putative fatty acid desaturase/cytochrome b5 fusion TC74979 AI484221 cLES1E11 XG3 T3M6 R19 C13 r2-c1 r4-c3 protein {Arabidopsis thaliana}PIR|A84900|A84900 sugar transporter like protein {Arabidopsis TC74988 AI777669 cLES2O22 XG12 T3M24 R1 C13 r2-c1 r4-c3 thaliana}GP|2464913|emb|CAB16808.1||Z99708 sugar transp putative UDP-glucose:glycoprotein glucosyltransferase; TC75003 AW030751 cLEC25H7 IF10 T1K19 R6 C11 r1-c2 r3-c3 101200-91134 {Arabidopsis thaliana}PIR|G9673 putative nucleotide-sugar transporter {Arabidopsis TC75014 AW219952 cLEX6M9 XIIIF4 T4K7 R18 C11 r2-c2 r1-c4 thaliana}PIR|E84509|E84509 probable vanadate res Putative UDP-glucose glucosyltransferase {Arabidopsis TC75032 AW621210 cLEX11K13 XIIIB4 T4C7 R18 C3 r2-c2 r1-c4 thaliana}PIR|H86356|H86356 probable UDP-gluco RING-H2 finger protein RHF2a {Arabidopsis TC75038 BE434274 cLEG15L16 VE8 T2I15 R12 C9 r4-c2 r1-c3 thaliana}GP|13374859|emb|CAC34493.1||AL589883 RING-H2 fin reticuline oxidase-like protein {Arabidopsis TC75058 AI771577 cLED30I10 IIIF4 T1L7 R18 C12 r1-c2 r3-c3 thaliana}GP|7268879|emb|CAB79083.1||AL161553 reticulin zinc finger protein-like {Arabidopsis thaliana} TC75079 BE461025 cLEG37C14 VID8 T2G16 R9 C7 r4-c2 r1-c3 contains similarity to ATPases associated with various TC75096 AI489887 cLED15P20 IIIA6 T1B11 R14 C2 r1-c2 r3-c3 cellular activities (Pfam: AAA.hmm, score: 15 contains similarity to phosphoenolpyruvate synthase TC75102 BE433957 cLEG9G8 VIIA5 T2B9 R16 C2 r4-c2 r1-c3 (ppsA) (GB: AE001056) {Arabidopsis thaliana}PIR| cytochrome P450 {Arabidopsis thaliana} TC75118 AI895885 cLEC10K8 IC1 T1E1 R24 C5 r1-c2 r3-c3 Similar to yeast general negative regulator of TC75146 AI895013 cLEC6F5 IIE6 T1I12 R13 C9 r1-c2 r3-c3 transcription subunit 1 {Arabidopsis thaliana}PIR|G8 putative cytochrome P450 {Oryza TC75173 BG135463 cTOE22L17 XVIIIE6 T5I12 R13 C9 r3-c2 r4-c4 sativa}GP|11761120|dbj|BAB19110.1||AP002839 putative cytochrome P45 nitrite reductase {Capsicum annuum} TC75187 BE451364 cLEY17P12 XIVA6 T4A12 R13 C1 r2-c2 r1-c4 tryptophan synthase beta chain {Arabidopsis thaliana} TC75190 AW625162 cLEZ11G16 XIVD1 T4G2 R23 C7 r2-c2 r1-c4 Contains a weak similarity to chalcone-flavonone TC75202 BE432201 cLEG6D8 VIH4 T2O8 R17 C15 r4-c2 r1-c3 isomerase from Pueraria lobata GP|Q43056 and conta similar to ATPases associated with various cellular TC75211 BE433089 cLEG12O3 VE1 T2I1 R24 C9 r4-c2 r1-c3 activites (Pfam: AAA.hmm, score: 230.91) {Arabid UTP-glucose glucosyltransferase {Arabidopsis thaliana} TC75218 BE432301 cLEG7K10 VIH9 T2O18 R7 C15 r4-c2 r1-c3 PROBABLE VACUOLAR ATP SYNTHASE TC75225 AW624381 cTOB15B21 XVIH11 T4P22 R3 C16 r2-c2 r1-c4 SUBUNIT H (EC 3.6.1.34) (V-ATPASE H SUBUNIT) (VACUOLAR PROTON PUMP H flavanone 3-hydroxylase-like protein {Arabidopsis TC75238 BF050330 cLEM17K22 VIIG12 T2N23 R2 C14 r4-c2 r1-c3 thaliana} isoflavone reductase-like protein {Arabidopsis TC75240 BF050320 cLEM17I14 VIIG11 T2N21 R4 C14 r4-c2 r1-c3 thaliana}GP|7270404|emb|CAB80171.1||AL161585 isoflav cystathionine beta-lyase {Solanum tuberosum} TC75245 BE460087 cLEM8N14 VIIIF9 T2L18 R7 C12 r4-c2 r1-c3 putative acyl-CoA synthetase; 62297-59022 TC75253 BE441105 cLEM1O7 VIIH11 T2P21 R4 C16 r4-c2 r1-c3 {Arabidopsis thaliana}PIR|D96805|D96805 probable acyl-CoA PHOSPHOGLUCOMUTASE, CHLOROPLAST TC75272 BE458570 cLEM2F21 VIIID2 T2H4 R21 C8 r4-c2 r1-c3 PRECURSOR (EC 5.4.2.2) (GLUCOSE PHOSPHOMUTASE) (PGM).GP|8250622|emb putative cytochrome P450 {Solanum TC75279 AW616136 cLHT6I5 XVD1 T4H1 R24 C8 r2-c2 r1-c4 chacoense}SP|P93531|C7D7_SOLCH CYTOCHROME P450 71D7 (EC 1.14.—.—) hydroxymethyltransferase {Arabidopsis TC75281 AW738537 cTOD7L23 XVIIIA9 T5A18 R7 C1 r3-c2 r4-c4 thaliana}GP|2244749|emb|CAB10172.1||Z97335 hydroxymethyltrans cytochrome P450, putative {Arabidopsis TC75284 AW651509 cLEI16L8 VIID2 T2H3 R22 C8 r4-c2 r1-c3 thaliana}PIR|F86441|F86441 probable cytochrome P450 [importe HD-Zip protein {Arabidopsis TC75348 AW035070 cLEC13O19 ID3 T1G5 R20 C7 r1-c2 r3-c3 thaliana}GP|3132474|gb|AAC16263.1||AC003096 homeodomain transcription f putative bZIP transcription factor {Arabidopsis TC75368 AW617711 cLHT24E20 XVB7 T4D13 R12 C4 r2-c2 r1-c4 thaliana}PIR|G84831|G84831 probable bZIP transcript putative phosphate/phosphoenolpyruvate translocator TC75371 AW617772 cLHT24B1 XVB4 T4D7 R18 C4 r2-c2 r1-c4 protein {Arabidopsis thaliana}PIR|D84649|D84649 myb-like protein {Arabidopsis TC75389 AW040511 cLET8M17 XIID1 T3H2 R23 C8 r2-c1 r4-c3 thaliana}PIR|T48253|T48253 myb-like protein- Arabidopsis thaliana putative glucosyltransferase {Arabidopsis TC75393 AW623996 cTOB13F6 XVIH5 T4P10 R15 C16 r2-c2 r1-c4 thaliana}PIR|H84786|H84786 probable glucosyltransferase [ tyrosine decarboxylase {Papaver TC75404 BE449397 cLHT31K16 XVC2 T4F3 R22 C6 r2-c2 r1-c4 somniferum}SP|P54771|TYD5_PAPSO TYROSINE/DOPA DECARBOXYLASE 5 [INCL Similar to gb|U44028 transcription factor CKC from TC75426 AW030921 cLEC5O13 IIE3 T1I6 R19 C9 r1-c2 r3-c3 Arabidopsis thaliana and contains two PF|00847 AP bZIP transcription factor 6 {Phaseolus vulgaris} TC75472 AW930815 cLEF41I7 IVF5 T1L10 R15 C12 r1-c2 r3-c3 HEAT SHOCK FACTOR PROTEIN 7 (HSF 7) (HEAT TC75476 AW931176 cLEF43B2 IVG1 T1N2 R23 C14 r1-c2 r3-c3 SHOCK TRANSCRIPTION FACTOR 7) (HSTF 7).GP|4539457|emb|CAB phosphoenolpyruvate carboxylase 1 {Gossypium TC75495 BG130811 cTOE1I10 XVIIID9 T5G18 R7 C7 r3-c2 r4-c4 hirsutum}GP|2266947|gb|AAB80714.1||AF008939 phosphoeno CYP82C1p {Glycine max}PIR|T05942|T05942 TC75545 BG132070 cTOE6A12 XVIIIF12 T5K24 R1 C11 r3-c2 r4-c4 cytochrome P450 82C1-soybean glucose-6-phosphate isomerase {Spinacia TC75577 AW222686 cLEN9E7 IXE1 T3I1 R24 C9 r2-c1 r4-c3 oleracea}PIR|T09153|T09153 glucose-6-phosphate isomerase (E cytochrome P450 {Solanum tuberosum} TC75602 BF176441 cLEZ20B1 XIVF10 T4K20 R5 C11 r2-c2 r1-c4 acetyl-CoA synthetase-like protein {Arabidopsis TC75606 AW092581 cLET20N2 XIF1 T3L1 R24 C12 r2-c1 r4-c3 thaliana} Similar to ribokinase {Arabidopsis TC75622 AW929172 cTOC6B19 XVIIE4 T5I7 R18 C9 r3-c2 r4-c4 thaliana}PIR|F86307|F86307 hypothetical protein AAD50017.1 [impo 3-phosphoshikimate 1-carboxyvinyltransferase TC75646 BG129236 cTOF23B2 XIXF7 T5L13 R12 C12 r3-c2 r4-c4 precursor (5-enolpyruvylshikimate-3-phosphate synthase) TRYPTOPHAN SYNTHASE BETA CHAIN 2 TC75671 AW031813 cLEC39L1 IID1 T1G2 R23 C7 r1-c2 r3-c3 PRECURSOR (EC 4.2.1.20).GP|2792520|gb|AAB97087.1||AF042320 tryptop cinnamoyl CoA reductase-like protein {Arabidopsis TC75675 BE463117 cTOC11G16 XVIIC5 T5E9 R16 C5 r3-c2 r4-c4 thaliana}PIR|T48643|T48643 cinnamoyl CoA reductas nucleotide diphosphate kinase Ia {Arabidopsis TC75705 AW096444 cLET38J7 XIG12 T3N23 R2 C14 r2-c1 r4-c3 thaliana}GP|6065740|emb|CAB58230.1||AJ012758 nucleoti diacylglycerol kinase ATDGK1 homolog {Arabidopsis TC75708 BF112916 cLEG43G7 VIG4 T2M8 R17 C13 r4-c2 r1-c3 thaliana}GP|6562306|emb|CAB62604.1||AL133421 diac adenosine kinase {Arabidopsis TC75729 AW091866 cLET16L10 IVE3 T1J6 R19 C10 r1-c2 r3-c3 thaliana}GP|7378610|emb|CAB83286.1||AL162751 adenosine kinase-like pr bZIP protein {Arabidopsis thaliana}PIR|T49227|T49227 TC75747 BF112845 cLEG42H1 XIH3 T3P5 R20 C16 r2-c1 r4-c3 bZIP protein —Arabidopsis thaliana transcription factor like protein {Arabidopsis TC75876 AI484729 cLED3D21 IIIH12 T1P23 R2 C16 r1-c2 r3-c3 thaliana}GP|2244999|emb|CAB10419.1||Z97341 transcrip putative RING zinc finger protein {Arabidopsis TC75892 AW039871 cLET13H5 XIC10 T3F19 R6 C6 r2-c1 r4-c3 thaliana}GP|6682260|gb|AAF23312.1|AC016661_37|AC0166 polyneuridine aldehyde esterase, putative; 10297-12282 TC75906 BG133780 cTOE14I21 XVIIIC7 T5E14 R11 C5 r3-c2 r4-c4 {Arabidopsis thaliana} glucose 6 phosphate/phosphate translocator-like protein TC75908 BG133380 cTOE12O11 XVIIIC1 T5E2 R23 C5 r3-c2 r4-c4 {Arabidopsis thaliana}PIR|T51467|T51467 glu leucine zipper transcription factor {Solanum TC75947 AW224429 cLEW2G3 XIIH8 T3P16 R9 C16 r2-c1 r4-c3 tuberosum}GP|575418|emb|CAA57894.1||X82544 leucine zip zinc finger protein-like {Arabidopsis thaliana} TC75949 AW618814 cLPT17I15 XVH4 T4P7 R18 C16 r2-c2 r1-c4 Strong similarity to the TATA binding protein- TC76006 AI781503 cLES16A15 IIG1 T1M2 R23 C13 r1-c2 r3-c3 associated factor from A. thaliana gb|Y13673. ESTs gb contains similarity to transcription TC76014 AW030833 cLEC22E16 IE11 T1I21 R4 C9 r1-c2 r3-c3 regulator~gene_id: MRG7.19 {Arabidopsis thaliana} putative beta-amylase {Oryza TC76034 AW735936 cTOA5B10 XVIE11 T4J22 R3 C10 r2-c2 r1-c4 sativa}GP|13489165|gb|AAK27799.1|AC022457_2|AC022457 putative beta-amy aspartate carbamoyltransferase-poj TC76045 AI773785 cLER8M9 XC10 T3E20 R5 C5 r2-c1 r4-c3 phosphate/phosphoenolpyruvate translocator protein- TC76052 BE431693 cLEG30O13 VIA5 T2A10 R15 C1 r4-c2 r1-c3 like {Arabidopsis thaliana} bZIP transcriptional activator RSG {Nicotiana tabacum} TC76055 BE435933 cLEG29D23 VH10 T2O19 R6 C15 r4-c2 r1-c3 soluble starch (bacterial glycogen) synthase {Solanum TC76060 BE434991 cLEG24J21 VG7 T2M13 R12 C13 r4-c2 r1-c3 tuberosum}SP|P93568|UGS2_SOLTU SOLUBLE GLYCOG RING zinc finger protein-like {Arabidopsis thaliana} TC76080 AW031045 cLEC13K8 ID1 T1G1 R24 C7 r1-c2 r3-c3 lipoxygenase {Zantedeschia aethiopica} TC76090 AI896460 cLEC15G13 ID6 T1G11 R14 C7 r1-c2 r3-c3 13-lipoxygenase {Solanum TC76097 AI773255 cLER5L12 XC2 T3E4 R21 C5 r2-c1 r4-c3 tuberosum}GP|1495802|emb|CAA65268.1||X96405 13- lipoxygenase {Solanum tuber phosphoribosylanthranilate isomerase {Arabidopsis TC76109 AI485822 cLED4C4 XIE9 T3J17 R8 C10 r2-c1 r4-c3 thaliana} glycine hydroxymethyltransferase (EC 2.1.2.1)-like TC76133 AI782600 cLES20I3 XG8 T3M16 R9 C13 r2-c1 r4-c3 protein {Arabidopsis thaliana}GP|7270156|emb|CAB aldose 1-epimerase-like protein {Arabidopsis thaliana} TC76138 AW399079 cLPT5N10 XVIB4 T4D8 R17 C4 r2-c2 r1-c4 Contains a bZIP transcription factor PF|00170 domain. TC76171 BE353406 cTOA19E21 XVIE3 T4J6 R19 C10 r2-c2 r1-c4 ESTs gb|R30400, gb|AA650964, gb|AI994521 come branched-chain alpha-keto acid decarboxylase E1 beta TC76174 BG131126 cTOE2L1 XVIIIF3 T5K6 R19 C11 r3-c2 r4-c4 unit {Arabidopsis thaliana}PIR|D96597|D9659 HYDROXYMETHYLGLUTARYL-COA SYNTHASE TC76206 BG134552 cTOE16B16 XD1 T3G2 R23 C7 r2-c1 r4-c3 (EC 4.1.3.5) (HMG-COA SYNTHASE) (3- HYDROXY-3-METHYLGLUTARYL COENZ PROBABLE (S)-2-HYDROXY-ACID OXIDASE, TC76210 BF051567 cLEM23B19 VIIIB8 T2D16 R9 C4 r4-c2 r1-c3 PEROXISOMAL 2 (EC 1.1.3.15) (GLYCOLATE OXIDASE 2) (GOX 2) (SHOR glycolate oxidase TC76211 cLES15G14 cLES15G14 XVG8 T4N15 R12 C14 r2-c2 r1-c4 s-adenosylmethionine decarboxylase proenzyme TC76213 BE436856 cLEG34M14 XXIH8 T6O15 R12 C15 r3-c1 r2-c4 (induced stolen tip protein tub13) {Solanum tuberosum} S-adenosyl-L-methionine synthetase TC76214 BG129352 cTOF24G21 IVG5 T1N10 R15 C14 r1-c2 r3-c3 lipoxygenase TC76225 AW222704 cLEN9G21 IXE2 T3I3 R22 C9 r2-c1 r4-c3 lipoxygenase (LOX) TC76226 BE435005 cLEG24P7 XXH11 T5P22 R3 C16 r3-c2 r4-c4 Contains PF|00249 Myb-like DNA-binding domain. TC76257 AW442417 cLEN22N18 IXC5 T3E9 R16 C5 r2-c1 r4-c3 EST gb|Z18152 comes from this gene. {Arabidopsis tha UDP-glucose pyrophosphorylase precursor {Solanum TC76266 BE458654 cLEM2P4 VIIID4 T2H8 R17 C8 r4-c2 r1-c3 tuberosum}PIR|JX0128|XNPOU UTP-glucose-1- phosphat hydroxycinnamoyl-CoA:tyramine N- TC76267 AW035768 cLEC36G5 IIB11 T1C22 R3 C3 r1-c2 r3-c3 (hydroxycinnamoyl)transferase {Capsicum annuum} hydroxycinnamoyl-CoA:tyramine N- TC76268 AI775981 cLER17K13 IXH2 T3O3 R22 C15 r2-c1 r4-c3 (hydroxycinnamoyl)transferase {Capsicum annuum} hydroxycinnamoyl-CoA:tyramine N- TC76269 AI777112 cLER20I22 IIF11 T1K22 R3 C11 r1-c2 r3-c3 (hydroxycinnamoyl)transferase {Capsicum annuum} hydroxycinnamoyl-CoA:tyramine N- TC76270 AI774541 cLER12J23 IXE7 T3I13 R12 C9 r2-c1 r4-c3 hydroxycinnamoyl)transferase {Capsicum annuum} tyramine hydroxycinnamoyltransferase {Nicotiana TC76271 AW624965 cLEZ9E23 XIVG10 T4M20 R5 C13 r2-c2 r1-c4 tabacum} tyramine hydroxycinnamoyltransferase {Nicotiana TC76272 AW221079 cLEF3P9 IVE7 T1J14 R11 C10 r1-c2 r3-c3 tabacum} putative transcription factor BTF3 (RNA polymerase B TC76286 AW624910 cLEZ8J8 XIVG7 T4M14 R11 C13 r2-c2 r1-c4 transcription factor 3); 26343-27201 {Arabidops putative transcription factor BTF3 (RNA polymerase B TC76287 AI778696 cLES6I17 XIA4 T3B7 R18 C2 r2-c1 r4-c3 transcription factor 3); 26343-27201 {Arabidops chloroplast triose phosphate translocator precursor (ctpt) TC76288 BG123350 cTOF1N9 XIXD8 T5H15 R12 C8 r3-c2 r4-c4 (e29) {Solanum tuberosum}SP|P29463|CPTR_(—) chloroplast triose phosphate translocator precursor (ctpt) TC76289 AW096697 cLET39J4 XIF7 T3L13 R12 C12 r2-c1 r4-c3 (e29) {Solanum tuberosum}SP|P29463|CPTR_(—) anthocyanin 5-O-glucosyltransferase {Petunia x TC76292 AW220874 cLEF2D12 IVE5 T1J10 R15 C10 r1-c2 r3-c3 hybrida} phosphoglycerate kinase, cytosolic {Nicotiana TC76300 BG123532 cTOF2O21 XIF8 T3L15 R12 C12 r2-c1 r4-c3 tabacum}SP|Q42962|PGKY_TOBAC PHOSPHOGLYCERATE KINASE, homeobox 1 protein{circumflex over ( )}{circumflex over ( )}class II knotted-like TC76313 BG126987 cTOF14E11 XIXA2 T5B3 R22 C2 r3-c2 r4-c4 homeodomain protein chorismate synthase 1 TC76324 BE436253 cLEG31O19 VIA11 T2A22 R3 C1 r4-c2 r1-c3 chorismate synthase 1 precursor 3-phosphate TC76325 BG128364 cTOF20K8 XIXD11 T5H21 R4 C8 r3-c2 r4-c4 phospholyase 1) {Lycopersicon esculentum}SP|Q42884|ARC1 chorismate synthase 1 precursor 3-phosphate TC76326 AI490294 cLED24N12 IIIC12 T1F23 R2 C6 r1-c2 r3-c3 phospholyase 1) {Lycopersicon esculentum}SP|Q42884|ARC1 cytosolic NADP-malic enzyme{circumflex over ( )}{circumflex over ( )}malate dehydrogenase TC76336 AI484269 cLES1A11 XG2 T3M4 R21 C13 r2-c1 r4-c3 ATP synthase gamma unit, chloroplast precursor TC76348 BE458757 cLEM4B17 VIIID6 T2H12 R13 C8 r4-c2 r1-c3 {Nicotiana tabacum}SP|P29790|ATPG_TOBAC ATP SYNTH zinc-finger protein {Petunia x TC76350 AI898415 cLED33G4 IIIG2 T1N3 R22 C14 r1-c2 r3-c3 hybrida}GP|439493|dbj|BAA05079.1||D26086 zinc- finger protein {Petuni fructokinase TC76354 AW224797 cLEY6M13 XIVC8 T4E16 R9 C5 r2-c2 r1-c4 ATP synthase beta unit, mitochondrial precursor TC76359 AW738375 cTOD7I21 IB1 T1C1 R24 C3 r1-c2 r3-c3 {Nicotiana plumbaginifolia}SP|P17614|ATP2_NICPL spermidine synthase TC76360 AI778176 cLES4M11 XH8 T3O16 R9 C15 r2-c1 r4-c3 cDNA~Strawberry pyruvate decarboxylase {Fragaria x TC76372 BF051258 cLEM22E9 VIIIB1 T2D2 R23 C4 r4-c2 r1-c3 ananassa}GP|10121330|gb|AAG13131.1|AF193791_1|AF oxoglutarate malate translocator {Solanum TC76379 BG125227 cTOF8C1 XXIIA5 T6A10 R15 C1 r3-c1 r2-c4 tuberosum}GP|1486472|emb|CAA68164.1||X99853 oxoglutarate aspartate aminotransferase glyoxysomal isozyme AAT1 TC76380 AW648048 cLEI3C6 VIID9 T2H17 R8 C8 r4-c2 r1-c3 precursor {Glycine max}PIR|T06136|T06136 aspart putative bZIP DNA-binding protein {Capsicum TC76385 BE431986 cLEG4N17 XXIC8 T6E15 R12 C5 r3-c1 r2-c4 chinense} ATP synthase B′ unit precursor {Spinacia TC76386 AI782445 cLES19K17 XG1 T3M2 R23 C13 r2-c1 r4-c3 pleracea}SP|P31853|ATPX_SPIOL ATP SYNTHASE B′ CHAIN PRE ATP synthase beta chain precursor (unit II) TC76387 BG127384 cTOF16G12 XIXA8 T5B15 R12 C2 r3-c2 r4-c4 {Arabidopsis thaliana}GP|2864617|emb|CAA16964.1||AL0 homeodomain-leucine zipper protein 57 {Glycine max} TC76389 AI490100 cLED22O23 IIIC8 T1F15 R12 C6 r1-c2 r3-c3 VACUOLAR ATP SYNTHASE SUBUNIT G 1 (EC TC76393 AW626384 cLEZ19P6 XIVF6 T4K12 R13 C11 r2-c2 r1-c4 3.6.1.34) (V-ATPASE G SUBUNIT 1) (VACUOLAR PROTON PUMP G SUBUN cytochrome p450 lxxii hydroxylase) (ge10h) TC76404 BE432714 cLEG10A1 VD3 T2G5 R20 C7 r4-c2 r1-c3 {Catharanthus roseus}SP|Q05047|CP72_CATRO CYTOCHROME P45 nucleoside diphosphate kinase {Pisum sativum} TC76406 AA824969 CT252 XVIC11 T4F22 R3 C6 r2-c2 r1-c4 proline oxidase precursor {Arabidopsis thaliana} TC76411 AI489806 cLED15D13 IIH12 T1O24 R1 C15 r1-c2 r3-c3 UDP-glucose dehydrogenase {Glycine TC76434 BG134455 cTOE16I24 XXH8 T5P16 R9 C16 r3-c2 r4-c4 max}SP|Q96558|UGDH_SOYBN UDP-GLUCOSE 6- DEHYDROGENASE (EC 1.1.1.2 UDP-glucose dehydrogenase {Arabidopsis thaliana} TC76435 AW399489 cLPT7B4 XVIB3 T4D6 R19 C4 r2-c2 r1-c4 UDP-glucose dehydrogenase-like protein {Arabidopsis TC76436 BE344437 cLEY2E3 XIVC6 T4E12 R13 C5 r2-c2 r1-c4 thaliana}PIR|T51527|T51527 UDP-glucose dehydrog lipoxygenase {Solanum TC76460 AW091732 cLET15B12 XID4 T3H7 R18 C8 r2-c1 r4-c3 tuberosum}GP|1407705|gb|AAB67865.1||U60202 lipoxygenase {Solanum tuberosum}P 3-ketoacyl-CoA thiolase {Arabidopsis TC76465 AI774269 cLER12I19 IXE6 T3I11 R14 C9 r2-c1 r4-c3 thaliana}GP|2981618|dbj|BAA25249.1||AB008855 3- ketoacyl-CoA th alanine aminotransferase {Arabidopsis TC76487 AW622240 cLEX14L9 XVIF1 T4L2 R23 C12 r2-c2 r1-c4 thaliana}GP|12325273|gb|AAG52580.1|AC016529_11| AC016529 putat malate synthase, glyoxysomal {Cucumis TC76489 AW649182 cLEI7K2 VIIG1 T2N1 R24 C14 r4-c2 r1-c3 sativus}SP|P08216|MASY_CUCSA MALATE SYNTHASE, GLYOXYSOMAL (EC putative 6-phosphogluconolactonase {Arabidopsis TC76497 AI484635 cLED2C20 IIIE6 T1J11 R14 C10 r1-c2 r3-c3 thaliana} 6-phosphogluconolactonase-like protein {Arabidopsis TC76498 BE436461 cLEG32O16 VIB2 T2C4 R21 C3 r4-c2 r1-c3 thaliana} putative cinnamyl alcohol dehydrogenase {Malus x TC76501 AI776221 cLER17H12 IIIC1 T1F1 R24 C6 r1-c2 r3-c3 domestica}PIR|T16995|T16995 probable cinnamyl-alco pyrophosphate-fructose 6-phosphate 1- TC76514 AW035056 cLEC21E3 XVH7 T4P13 R12 C16 r2-c2 r1-c4 phosphotransferase alpha unit (pfp) (6- phosphofructokinase pyrophosphate--fructose 6-phosphate 1- TC76515 AW649519 cLEI8D13 VIIG2 T2N3 R22 C14 r4-c2 r1-c3 phosphotransferase alpha unit (pfp) (6- phosphofructokinase triosephosphate isomerase chloroplast precursor TC76528 AW094307 cLET28M15 XIG7 T3N13 R12 C14 r2-c1 r4-c3 {Spinacia oleracea}SP|P48496|TPIC_SPIOL TRIOSEPHOSP MALATE DEHYDROGENASE [NADP], TC76554 AI776445 cLER18D3 IXH4 T3O7 R18 C15 r2-c1 r4-c3 CHLOROPLAST PRECURSOR (EC 1.1.1.82) (NADP- MDH).GP|2827076|gb|AAB99753. succinyl-CoA-ligase beta unit {Arabidopsis TC76558 AI777206 cLER20L19 XB5 T3C10 R15 C3 r2-c1 r4-c3 thaliana}GP|6598664|gb|AAD25643.2|AC007109_1|AC007109 caffeoyl-CoA O-methyltransferase 5 {Nicotiana TC76559 BF176405 cLEZ20I22 XIVF12 T4K24 R1 C11 r2-c2 r1-c4 tabacum}GP|1679853|emb|CAB05369.1||Z82982 caffeoyl-Co fructokinase, putative {Arabidopsis TC76564 AW650710 cLEI13J20 VIIC1 T2F1 R24 C6 r4-c2 r1-c3 thaliana}GP|12324405|gb|AAG52172.1|AC020665_17| AC020665 fructok transcription factor TEIL {Nicotiana tabacum} TC76569 AI781500 cLES15H21 XE4 T3I8 R17 C9 r2-c1 r4-c3 putative phospholipid cytidylyltransferase {Arabidopsis TC76594 AW030340 cLEC16F23 IVE12 T1J24 R1 C10 r1-c2 r3-c3 thaliana}PIR|H84807|H84807 probable phospho S-adenosylmethionine:2-demethylmenaquinone TC76601 AI897772 cLED30J21 IIIF5 T1L9 R16 C12 r1-c2 r3-c3 methyltransferase-like protein {Arabidopsis thaliana} fructose-1,6-bisphosphatase precursor {Solanum TC76605 BG124012 cTOF3J20 XXD11 T5H22 R3 C8 r3-c2 r4-c4 tuberosum} Similar to gb|D86180 phosphoribosylanthranilate TC76611 AW039366 cLET9I8 XXIA8 T6A15 R12 C1 r3-c1 r2-c4 transferase from Pisum sativum and contains 2 PF|001 VACUOLAR ATP SYNTHASE 16 KDA TC76632 AI778869 cLES6M24 IXC9 T3E17 R8 C5 r2-c1 r4-c3 PROTEOLIPID SUBUNIT (EC 3.6.1.34) (V-ATPASE 16 KDA PROTEOLIPID SUBUNIT glutamate 1-semialdehyde 2,1-aminomutase TC76649 BG128388 cTOF20B1 XIXD10 T5H19 R6 C8 r3-c2 r4-c4 FRUCTOSE-1,6-BISPHOSPHATASE, TC76659 BG642995 cTOF26E6 XVIIE1 T5I1 R24 C9 r3-c2 r4-c4 CHLOROPLAST PRECURSOR (EC 3.1.3.11) (D- FRUCTOSE-1,6-BISPHOSPHATE 1-PHOS Similar to transaldolase {Arabidopsis TC76672 BG127427 cTOF16B1 VA12 T2A23 R2 C1 r4-c2 r1-c3 thaliana}PIR|D86257|D86257 hypothetical protein [imported]- CYP94A1 {Vicia sativa}PIR|T08014|T08014 TC76678 BE458460 cLEM2K13 VIIID3 T2H6 R19 C8 r4-c2 r1-c3 cytochrome P450 CYP94A1-spring vetch 2-isopropylmalate synthase {Lycopersicon TC76694 AW441463 cLEN17E12 IXA11 T3A21 R4 C1 r2-c1 r4-c3 pennellii}SP|O04973|LU1A_LYCPN 2- ISOPROPYLMALATE SYNTHASE putative cinnamoyl-CoA reductase {Arabidopsis TC76707 AW093204 cLET24C11 XIF9 T3L17 R8 C12 r2-c1 r4-c3 thaliana}PIR|D84747|D84747 probable cinnamoyl-CoA red putative nucleotide-sugar dehydratase {Arabidopsis TC76708 AI483494 cLED24I2 IIIC11 T1F21 R4 C6 r1-c2 r3-c3 thaliana}PIR|T00419|T00419 dTDP-glucose 4-6-dehy zinc finger protein {Arabidopsis thaliana} TC76725 AI782757 cLES20O10 XXIH3 T6O5 R20 C15 r3-c1 r2-c4 transcription factor Hap5a-like protein {Arabidopsis TC76772 AI778935 cLES6J13 IB7 T1C13 R12 C3 r1-c2 r3-c3 thaliana} cytochrome c oxidase unit 6b-1 {Oryza TC76784 AI776716 cLER19H17 XXIG7 T6M13 R12 C13 r3-c1 r2-c4 sativa}GP|9967277|dbj|BAB12338.1||AB047975 cytochrome c ox beta-fructofuranosidase (invertase){circumflex over ( )}{circumflex over ( )}beta- TC76785 AI489825 cLED15G4 IIIA4 T1B7 R18 C2 r1-c2 r3-c3 fructosidase{circumflex over ( )}{circumflex over ( )}beta fructosidase ATP synthase delta unit, chloroplast precursor TC76808 AI772236 cLER2G15 XB7 T3C14 R11 C3 r2-c1 r4-c3 {Nicotiana tabacum}SP|P32980|ATPD_TOBAC ATP SYNTH aminotransferase-like protein {Arabidopsis thaliana} TC76819 BG130515 cTOF30H11 XXB10 T5D20 R5 C4 r3-c2 r4-c4 contains similarity to C2H2-type zinc finger TC76821 AI778334 cLES5A19 IVF2 T1L4 R21 C12 r1-c2 r3-c3 protein~gene_id: MOK16.6 {Arabidopsis thaliana} NADH-cytochrome b5 reductase {Arabidopsis TC76827 BF113582 cLEY21D5 XIVB7 T4C14 R11 C3 r2-c2 r1-c4 thaliana}GP|4240118|dbj|BAA74838.1||AB007800 NADH-cytochr lipoxygenase TC76842 BF050599 cLEM18P7 VIIH3 T2P5 R20 C16 r4-c2 r1-c3 Similar to dTDP-D-glucose 4,6-dehydratase TC76851 BF051373 cLEM22N13 IVF12 T1L24 R1 C12 r1-c2 r3-c3 {Arabidopsis thaliana}PIR|C96814|C96814 hypothetical prot UDP-glucose:salicylic acid glucosyltransferase TC76866 AI490565 cLED25E6 IIID5 T1H9 R16 C8 r1-c2 r3-c3 {Nicotiana tabacum} putative cytochrome P450 {Arabidopsis TC76887 AW223851 cLEN13J16 VIIIH5 T2P10 R15 C16 r4-c2 r1-c3 thaliana}GP|13877669|gb|AAK43912.1|AF370593_1|AF370593 putati contains similarity to shikimate kinase TC76889 AI781256 cLES14N4 XD12 T3G24 R1 C7 r2-c1 r4-c3 precursor~gene_id: MDJ14.24 {Arabidopsis thaliana} contains similarity to RING zinc finger TC76902 BG129834 cTOF28B1 XXA7 T5B14 R11 C2 r3-c2 r4-c4 protein~gene_id: MBD2.14 {Arabidopsis thaliana} alpha-glucan phosphorylase, h isozyme phosphorylase TC76936 AW093686 cLET25F14 XIG3 T3N5 R20 C14 r2-c1 r4-c3 h) {Solanum tuberosum}SP|P32811|PHSH_SOLTU ALPH CTP:phosphocholine cytidylyltransferase {Brassica TC76939 BE458926 cLEM5C9 XVIA2 T4B4 R21 C2 r2-c2 r1-c4 napus}GP|1416514|dbj|BAA09644.1||D63168 CTP:phosp citrate synthase {Nicotiana TC76947 AI781385 cLES15O17 XE5 T3I10 R15 C9 r2-c1 r4-c3 tabacum}EGAD|126596|143593 citrate synthase {Nicotiana tabacum}GP|2300 nucleoside diphosphate kinase II precursor {Spinacia TC76957 BG123962 cTOF3P9 XXIIA1 T6A2 R23 C1 r3-c1 r2-c4 oleracea}SP|Q01402|NDK2_SPIOL NUCLEOSIDE DIPHO delta 1-pyrroline-5-carboxylate synthetase TC76960 BF112629 cLEG41P2 XXIG8 T6M15 R12 C13 r3-c1 r2-c4 ferritin unit cowpea2 precursor {Vigna TC76962 BE460085 cLEM8N10 VIIIF8 T2L16 R9 C12 r4-c2 r1-c3 unguiculata}PIR|T08124|T08124 ferritin 2 precursor- cowp tomato invertase inhibitor TC76975 AW039904 cLET13B14 VA4 T2A7 R18 C1 r4-c2 r1-c3 chalcone--flavanone isomerase a {Petunia TC76987 AI485187 cLED5C15 IVA10 T1B20 R5 C2 r1-c2 r3-c3 hybrida}SP|P11650|CFIA_PETHY CHALCONE-- FLAVONONE ISOMERASE 3-ketoacyl-CoA thiolase {Arabidopsis TC76988 AI781985 cLES17D18 XXID11 T6G21 R4 C7 r3-c1 r2-c4 thaliana}GP|2981618|dbj|BAA25249.1||AB008855 3- ketoacyl-CoA th chalcone synthase TC77000 BG128271 cTOF19H11 XIXC6 T5F11 R14 C6 r3-c2 r4-c4 contains similarity to diaminopimelate TC77005 AW224158 cLEN16M11 IXA9 T3A17 R8 C1 r2-c1 r4-c3 decarboxylase~gene_id: MLN21.17 {Arabidopsis thaliana} glyceraldehyde 3-phosphate dehydrogenase TC77013 AI779651 cLES8P13 XXIC12 T6E23 R2 C5 r3-c1 r2-c4 aspartate aminotransferase {Medicago TC77015 BE463395 cTOC12P16 XVIIC10 T5E19 R6 C5 r3-c2 r4-c4 sativa}□GP|777387|gb|AAB46611.1||L25335 aspartate aminotransfer Contains similarity to a putative 6- TC77016 AW399260 cLPT6D18 XVIB8 T4D16 R9 C4 r2-c2 r1-c4 phosphogluconolactonase T1G12.6 GP|6553917 from Arabidopsis thal WRKY transcription factor Nt-SubD48 {Nicotiana TC77024 BG626344 cLEL11P19 XXIB3 T6C5 R20 C3 r3-c1 r2-c4 tabacum} glutamate decarboxylase isozyme 4 {Nicotiana TC77052 AW030971 cLEC5E1 IID12 T1G24 R1 C7 r1-c2 r3-c3 tabacum} D-3-PHOSPHOGLYCERATE DEHYDROGENASE TC77066 AW625643 cLEZ16I8 XXH2 T5P4 R21 C16 r3-c2 r4-c4 PRECURSOR (EC 1.1.1.95) (PGDH).GP|2189964|dbj|BAA20405.1||AB0032 putative glucosyl transferase {Arabidopsis TC77071 BE432435 cLEG8C10 VIE4 T2I8 R17 C9 r4-c2 r1-c3 thaliana}PIR|H84784|H84784 probable glucosyl transferase 11S globulin precursor {Sesamum indicum} TC77083 AI489377 cLED17A13 IVD6 T1H12 R13 C8 r1-c2 r3-c3 Putative ABC transporter {Arabidopsis TC77089 AW222251 cLEN7O6 IVH10 T1P20 R5 C16 r1-c2 r3-c3 thaliana}PIR|H96622|H96622 probable ABC transporter F23H11.19 putative fatty acid desaturase {Arabidopsis TC77096 AI772259 cLER2K17 XB8 T3C16 R9 C3 r2-c1 r4-c3 thaliana}GP|4325341|gb|AAD17340.1||AF128393 similar to S-adenosyl-L-methionine:salicylic acid carboxyl TC77118 AI487371 cLED13G8 IIH5 T1O10 R15 C15 r1-c2 r3-c3 methyltransferase {Stephanotis floribunda} putative hydroxymethylglutaryl-CoA lyase protein TC77127 AW222487 cLEN8G12 IXD8 T3G15 R12 C7 r2-c1 r4-c3 {Arabidopsis thaliana}GP|13194812|gb|AAK15568.1|AF PYRROLINE-5-CARBOXYLATE REDUCTASE (EC TC77132 AI485470 cLED4L3 IVA7 T1B14 R11 C2 r1-c2 r3-c3 1.5.1.2) (P5CR) (P5C REDUCTASE).GP|1928962|gb|AAC14482.1||U92 putative transcription factor {Oryza TC77133 BG124550 cTOF5G18 XXIA12 T6A23 R2 C1 r3-c1 r2-c4 sativa}GP|12328532|dbj|BAB21190.1||AP002909 putative transcrip S-adenosylmethionine:2-demethylmenaquinone TC77161 BG129691 cTOF27J12 XXA3 T5B6 R19 C2 r3-c2 r4-c4 methyltransferase-like {Arabidopsis thaliana} UDP rhamnose: anthocyanidin-3-glucoside TC77166 BF051960 cLEM24D18 VIIIC2 T2F4 R21 C6 r4-c2 r1-c3 rhamnosyltransferase {Petunia x hybrida}PIR|S36655|S36655 U phosphoenolpyruvate carboxylase kinase TC77168 BG129025 cTOF23I5 XIXF11 T5L21 R4 C12 r3-c2 r4-c4 putative aspartate aminotransferase {Arabidopsis TC77175 AW738611 cTOD7N10 XVIIIA10 T5A20 R5 C1 r3-c2 r4-c4 thaliana}PIR|E84610|E84610 probable aspartate amin ADP-glucose pyrophosphorylase large unit TC77179 AI782268 cLES18L13 XF10 T3K20 R5 C11 r2-c1 r4-c3 threonine synthase {Solanum tuberosum} TC77196 BG127194 cTOF14P1 XIXA7 T5B13 R12 C2 r3-c2 r4-c4 tryptophan synthase beta chain {Arabidopsis thaliana} TC77225 BG135503 cTOE22D24 XVIIIE4 T5I8 R17 C9 r3-c2 r4-c4 putative C3HC4-type RING zinc finger/ankyrin protein TC77229 BG126573 cTOF12P19 VA10 T2A19 R6 C1 r4-c2 r1-c3 {Arabidopsis thaliana}PIR|E84689|E84689 probab UMP/CMP kinase like protein {Arabidopsis TC77240 AI486780 cLED11D6 IIG9 T1M18 R7 C13 r1-c2 r3-c3 thaliana}GP|7269379|emb|CAB81339.1||AL161563 UMP/CMP kinas PROBABLE UDP-GLUCOSE 4-EPIMERASE TC77242 AW649490 cLEI8K18 VIIG3 T2N5 R20 C14 r4-c2 r1-c3 AT4G23920 (EC 5.1.3.2) (GALACTOWALDENASE) (UDP-GALACTOSE 4-EPIMERAS putative zinc finger protein {Oryza sativa} TC77251 AW929282 cTOC7K15 VD1 T2G1 R24 C7 r4-c2 r1-c3 fructose-1,6-biphosphatase TC77264 BG128077 cTOF18N18 IVH11 T1P22 R3 C16 r1-c2 r3-c3 shikimate kinase precursor TC77265 AW738270 cTOD6F10 XVIIIA2 T5A4 R21 C1 r3-c2 r4-c4 shikimate kinase precursor {Lycopersicon TC77266 BF113149 cLEG43N23 VIG5 T2M10 R15 C13 r4-c2 r1-c3 esculentum}SP|Q00497|AROK_LYCES SHIKIMATE KINASE PRECURSOR putative sugar transporter TC77279 AW928958 cTOC4G10 XVIID9 T5G17 R8 C7 r3-c2 r4-c4 S-adenosyl-L-methionine:salicylic acid carboxyl TC77297 AW928688 cTOC2F6 XVIID5 T5G9 R16 C7 r3-c2 r4-c4 methyltransferase {Atropa belladonna} G-box binding protein TC77305 AW737133 cTOD2M3 XVIIG5 T5M9 R16 C13 r3-c2 r4-c4 unnamed protein product TC77310 BG643583 cTOF31O17 XXC8 T5F16 R9 C6 r3-c2 r4-c4 {unidentified}GP|6683619|dbj|BAA89269.1||AB025250 ATP phosphoribosyl transf putative NADH dehydrogenase (ubiquinone TC77318 AI486928 cLED6L17 IVB11 T1D22 R3 C4 r1-c2 r3-c3 oxidoreductase) {Arabidopsis thaliana}PIR|T02486|T02486 hyp contains similarity to transcription TC77334 BG643422 cTOF27H23 XXA2 T5B4 R21 C2 r3-c2 r4-c4 regulator~gene_id: MRG7.19 {Arabidopsis thaliana} G-box binding protein TC77337 cLEN12J21 cLEN12J21 IVE2 T1J4 R21 C10 r1-c2 r3-c3 NADH dehydrogenase {Solanum TC77343 AI490708 cLEI15H12 IA11 T1A21 R4 C1 r1-c2 r3-c3 tuberosum}SP|P80269|NUIM_SOLTU NADH- UBIQUINONE OXIDOREDUCTASE 23 KDA SU phosphatidylserine decarboxylase {Arabidopsis TC77346 AW616501 cLHT11D21 XIVH3 T4O6 R19 C15 r2-c2 r1-c4 thaliana} bHLH transcription factor JAF13 {Petunia x hybrida} TC77374 AI490451 cLED21H12 XXIG1 T6M1 R24 C13 r3-c1 r2-c4 nitrite reductase {Capsicum annuum} TC77375 BE449918 cLEY11I6 XIIIF12 T4K23 R2 C11 r2-c2 r1-c4 putative aminotransferase; 101422-99564 {Arabidopsis TC77383 AW040370 cLET3A15 XIH7 T3P13 R12 C16 r2-c1 r4-c3 thaliana}PIR|D96806|D96806 probable aminotrans VACUOLAR ATP SYNTHASE 16 KDA TC77384 BG128906 cTOF22P23 XIXF5 T5L9 R16 C12 r3-c2 r4-c4 PROTEOLIPID SUBUNIT (EC 3.6.1.34) (V-ATPASE 16 KDA PROTEOLIPID SUBUNIT cytochrome c oxidase unit Vb precursor-like protein TC77386 BG125994 cTOF10J17 XVIIIG7 T5M14 R11 C13 r3-c2 r4-c4 {Arabidopsis thaliana} PROBABLE RIBOSE 5-PHOSPHATE ISOMERASE TC77390 AW623788 cTOB13K7 XVIH8 T4P16 R9 C16 r2-c2 r1-c4 (EC 5.3.1.6) (PHOSPHORIBOISOMERASE).GP|4262236|gb|AAD14529.1| phosphoenolpyruvate carboxylase 1 TC77403 AI781699 cLES16H4 XE10 T3I20 R5 C9 r2-c1 r4-c3 nitrite reductase {Capsicum annuum} TC77408 AW219345 cLEX4I13 XIIIE7 T4I13 R12 C9 r2-c2 r1-c4 hypothetical protein {Arabidopsis TC77438 AW649316 cLEI7H24 XIVB1 T4C2 R23 C3 r2-c2 r1-c4 thaliana}GP|3281856|emb|CAA19751.1||AL031004 Transcription factor putative glucose-6-phosphate/phosphate-tranlocat or TC77448 AW034294 cLEC37H6 IVE6 T1J12 R13 C10 r1-c2 r3-c3 {Oryza sativa} uroporphyrinogen decarboxylase precursor {Nicotiana TC77455 AW929502 cTOC9I7 XVIIF8 T5K15 R12 C11 r3-c2 r4-c4 tabacum}SP|Q42967|DCUP_TOBAC UROPORPHYRINOGEN D putative strictosidine synthase; 35901-37889 TC77457 BG126446 cTOF12I4 XVIIIH6 T5O12 R13 C15 r3-c2 r4-c4 {Arabidopsis thaliana}PIR|A96768|A96768 protein strict putative aminotransferase {Arabidopsis thaliana} TC77480 AI897400 cLED27I4 IIIH8 T1P15 R12 C16 r1-c2 r3-c3 TRANSCRIPTION INITIATION FACTOR TFIID 100 KDA TC77486 BE435714 cLEG28M12 VH8 T2O15 R12 C15 r4-c2 r1-c3 SUBUNIT (TAFII-100) (TAFII100).GP|1932938|gb|AAC51215 putative glucosyl transferase {Arabidopsis TC77491 AI487582 cLED9F15 IVC10 T1F20 R5 C6 r1-c2 r3-c3 thaliana}PIR|C84784|C84784 probable glucosyl transferase glucose-6-phosphate 1-dehydrogenase {Solanum TC77502 BE431600 cLEG27K21 XIIIE12 T4I23 R2 C9 r2-c2 r1-c4 tuberosum}SP|P37830|G6PD_SOLTU GLUCOSE-6- PHOSPHATE 1-D omega-6 fatty acid desaturase {Sesamum indicum} TC77526 AI895164 cLEC6P16 IH12 T1O23 R2 C15 r1-c2 r3-c3 putative C3HC4-type RING zinc finger protein TC77528 AW223270 cLEN11E11 VIIIG4 T2N8 R17 C14 r4-c2 r1-c3 {Arabidopsis thaliana}PIR|T02413|T02413 probable RING Alfin-1 {Medicago sativa}PIR|T09646|T09646 probable TC77531 AI895907 cLEC10O8 XXID4 T6G7 R18 C7 r3-c1 r2-c4 zinc finger protein-alfalfa (fragment) putative ABC transporter; 66585-65723 {Arabidopsis TC77538 AW621599 cLEX12D20 XIIIB10 T4C19 R6 C3 r2-c2 r1-c4 thaliana}PIR|C96702|C96702 probable ABC transpor phosphoribosyl pyrophosphate synthase isozyme 3 TC77539 AI776625 cLER19A6 IXH10 T3O19 R6 C15 r2-c1 r4-c3 {Spinacia oleracea} TRYPTOPHAN SYNTHASE BETA CHAIN 2 TC77555 AI488733 cLED13J19 IIH7 T1O14 R11 C15 r1-c2 r3-c3 PRECURSOR (EC 4.2.1.20).GP|2792520|gb|AAB97087.1||AF042320 tryptop indole-3-glycerol phosphate synthase {Arabidopsis TC77561 AW033644 cLEC29B10 IG9 T1M17 R8 C13 r1-c2 r3-c3 thaliana} cytochrome P450 {Solanum tuberosum} TC77562 AW648014 cLEI3K17 VIID11 T2H21 R4 C8 r4-c2 r1-c3 acetyl-CoA carboxylase {Medicago TC77572 AW040576 cLET7G16 XIIC2 T3F4 R21 C6 r2-c1 r4-c3 sativa}GP|495725|gb|AAB42144.1||L25042 acetyl-CoA carboxylase {Med 3-isopropylmalate dehydratase, small unit TC77576 BG131961 cTOE5J4 XXIIA8 T6A16 R9 C1 r3-c1 r2-c4 {Arabidopsis thaliana}PIR|H84861|H84861 3- isopropylmal MADS-box transcription factor FBP22 {Petunia x TC77597 AI486684 cLED11H18 IIG11 T1M22 R3 C13 r1-c2 r3-c3 hybrida} probable UDP-glucuronosyltransferase (EC 2.4.1.—) — TC77599 AI898207 cLED32E12 IIIF12 T1L23 R2 C12 r1-c2 r3-c3 garden pea NADH dehydrogenase {Solanum TC77602 BG124296 cTOF4H14 XXE5 T5J10 R15 C10 r3-c2 r4-c4 tuberosum}GP|639834|emb|CAA58823.1||X83999 NADH dehydrogenase {Solanum phosphoglucomutase-like protein {Arabidopsis TC77603 AW038594 cLET7O17 XIIC5 T3F10 R15 C6 r2-c1 r4-c3 thaliana}PIR|T51457|T51457 phosphoglucomutase-like pro biotin-binding protein{circumflex over ( )}{circumflex over ( )}biotin-containing unit of TC77606 BG128249 cTOF19D1 XIXC4 T5F7 R18 C6 r3-c2 r4-c4 methylcrotonyl-CoA carboxylase ATP:citrate lyase {Capsicum annuum} TC77626 BG127685 cTOF17F3 XIXB2 T5D3 R22 C4 r3-c2 r4-c4 putative cytochrome P450 {Solanum TC77648 AI485818 cLED4O17 IVA8 T1B16 R9 C2 r1-c2 r3-c3 chacoense}SP|P93530|C7D6_SOLCH CYTOCHROME P450 71D6 (EC 1.14.—.—) cytochrome c oxidase unit 6b {Oryza TC77660 AI775016 cLER14G1 IXF4 T3K7 R18 C11 r2-c1 r4-c3 sativa}GP|9967162|dbj|BAB12275.1||AB047923 cytochrome c oxid glycerol-3-phosphate acyltransferase {Cucumis TC77666 BE449429 cLHT31D3 XVC1 T4F1 R24 C6 r2-c2 r1-c4 sativus}SP|Q39639|PLSB_CUCSA GLYCEROL-3- PHOSPHATE ACY S-adenosyl-L-methionine:salicylic acid carboxyl TC77684 BE354257 cTOD9B6 XVIIIB4 T5C8 R17 C3 r3-c2 r4-c4 methyltransferase-like protein {Arabidopsis thaliana 3-deoxy-D-arabino-heptulosonate 7-phosphate synthase TC77693 AW091589 cLET15J4 XVIE5 T4J10 R15 C10 r2-c2 r1-c4 {Morinda citrifolia} serine hydroxymethyltransferase, mitochondrial TC77724 BG126939 cTOF13L12 XVIIIH10 T5O20 R5 C15 r3-c2 r4-c4 precursor (serine methylase) (glycine hydroxymethyltr putative sugar transporter {Arabidopsis thaliana} TC77728 AI490207 cLER1M15 XA9 T3A18 R7 C1 r2-c1 r4-c3 alpha-glucan phosphorylase, 1 isozyme 2 precursor TC77734 BG644107 cTOF34I23 XXD6 T5H12 R13 C8 r3-c2 r4-c4 (starch phosphorylase 1-2) {Solanum tuberosum}SP| HB2 homeodomain protein {Populus tremula x Populus TC77747 AW945094 cTOB16M6 XVIIA7 T5A13 R12 C1 r3-c2 r4-c4 tremuloides} Strong similarity to gb|U61231 cytochrome P450 from TC77757 BG125277 cTOF8K13 XXG6 T5N12 R13 C14 r3-c2 r4-c4 Arabidopsis thaliana and is a member of the PF|0 succinyl-CoA synthetase, alpha unit {Arabidopsis TC77763 BE451337 cLEY17J6 XIVA4 T4A8 R17 C1 r2-c2 r1-c4 thaliana} NADH dehydrogenase {Solanum TC77792 AW623479 cTOB10F18 XVIF12 T4L24 R1 C12 r2-c2 r1-c4 tuberosum}GP|639834|emb|CAA58823.1||X83999 NADH dehydrogenase {Solanum glucose-6-phosphate/phosphate-translocator precursor TC77793 AW399232 cLPT6N15 XVIB12 T4D24 R1 C4 r2-c2 r1-c4 {Pisum sativum}PIR|T06254|T06254 glucose-6-pho pyrophosphate--fructose 6-phosphate 1- TC77808 BG643516 cTOF31A1 XXC1 T5F2 R23 C6 r3-c2 r4-c4 phosphotransferase alpha unit (pfp) (6- phosphofructokinase adenosine kinase {Arabidopsis TC77810 BE450032 cLEY11D12 XIIIF9 T4K17 R8 C11 r2-c2 r1-c4 thaliana}GP|7378610|emb|CAB83286.1||AL162751 adenosine kinase-like pr sucrose transporter {Lycopersicon esculentum} TC77814 AW650849 cLEI14L5 VB3 T2C5 R20 C3 r4-c2 r1-c3 transketolase 1 {Capsicum TC77838 AI780217 cLES11I1 XIVA3 T4A6 R19 C1 r2-c2 r1-c4 annuum}PIR|T09541|T09541 transketolase (EC 2.2.1.1) TKT1 precursor, chlor transcription factor inhibitor I kappa B homolog TC77842 AW160234 cLPT1I9 XIID11 T3H22 R3 C8 r2-c1 r4-c3 {Arabidopsis thaliana}GP|1773295|gb|AAC49611.1||U7 aspartate-semialdehyde dehydrogenase precursor TC77844 BG134476 cTOE16M18 XVIIID1 T5G2 R23 C7 r3-c22 r4-c4 {Arabidopsis thaliana} putative flavonol 3-O-glucosyltransferase {Arabidopsis TC77847 BG127210 cTOF14B18 XIXA1 T5B1 R24 C2 r3-c2 r4-c4 thaliana}PIR|F84618|F84618 probable flavonol ornithine carbamoyltransferase; OCTase {Canavalia TC77862 AW222161 cLEN7K19 IXD7 T3G13 R12 C7 r2-c1 r4-c3 lineata}GP|12003188|gb|AAG43481.1|AF203688_1|AF20 NADH-dependent glutamate synthase {Medicago TC77867 AW616998 cLHT19G12 XVA9 T4B17 R8 C2 r2-c2 r1-c4 sativa} contains similarity to transcription TC77873 BG124285 cTOF4F12 XXE2 T5J4 R21 C10 r3-c2 r4-c4 regulator~gene_id: MRG7.19 {Arabidopsis thaliana} contains similarity to C2H2-type zinc finger TC77881 BG123144 cTOF1C1 XIXC11 T5F21 R4 C6 r3-c2 r4-c4 protein~gene_id: MOK16.6 {Arabidopsis thaliana} putative zinc finger protein {Oryza sativa} TC77907 AI782007 cLES17H16 XF3 T3K6 R19 C11 r2-c1 r4-c3 putative hydroxymethyltransferase; 49598-47322 TC77914 AW220191 cLEX8O6 XIIIF7 T4K13 R12 C11 r2-c2 r1-c4 {Arabidopsis thaliana}PIR|F86484|F86484 probable hyd deoxyuridine triphosphatase; dUTPase, P18 {EC TC77923 AI487253 cLED11P16 IIH3 T1O6 R19 C15 r1-c2 r3-c3 3.6.1.23} [tomatoes, Tint Tim cultivar LA154, Peptide, 169 aa] cytochrome P450, putative {Arabidopsis TC77959 BG123929 cTOF3J9 XXD12 T5H24 R1 C8 r3-c2 r4-c4 thaliana}PIR|F86441|F86441 probable cytochrome P450 [importe NAD-malate dehydrogenase {Nicotiana tabacum} TC77971 AW648430 cLEI4F3 VIIE7 T2J13 R12 C10 r4-c2 r1-c3 aspartate aminotransferase {Panicum TC77973 AI484604 cLED2E7 IIIE7 T1J13 R12 C10 r1-c2 r3-c3 miliaceum}GP|20597|emb|CAA45022.1||X63428 aspartate aminotransf phosphoenolpyruvate carboxylase {Nicotiana TC77975 AI897765 cLED30H23 IIIF3 T1L5 R20 C12 r1-c2 r3-c3 tabacum}SP|P27154|CAPP_TOBAC PHOSPHOENOLPYRUVATE CARBOXY Contains similarity to DNA-binding protein MYB1 TC77983 BG127613 cTOF17E20 XIXB1 T5D1 R24 C4 r3-c2 r4-c4 from Petroselinum crispum GP|7488946 and contains MY phosphatidylinositol 4-kinase {Solanum tuberosum} TC78010 AI782370 cLES18N16 XF11 T3K22 R3 C11 r2-c1 r4-c3 L-allo-threonine aldolase homolog F22O13.11- TC78023 AW737305 cTOD3I3 XVIIG10 T5M19 R6 C13 r3-c2 r4-c4 Arabidopsis thaliana argininosuccinate synthase-like protein {Arabidopsis TC78033 BE458353 cLEM1H12 VIIH9 T2P17 R8 C16 r4-c2 r1-c3 thaliana}GP|7269334|emb|CAB79393.1||AL161562 a hyoscyamine 6-dioxygenase hydroxylase, putative TC78043 BE436223 cLEG31I23 VIA8 T2A16 R9 C1 r4-c2 r1-c3 {Arabidopsis thaliana}PIR|G86472|G86472 probable hy SNF2 family global transcription activator TC78051 BF097336 cLEW20A10 XIIF12 T3L24 R1 C12 r2-c1 r4-c3 {Arabidopsis thaliana}PIR|G84897|G84897 hypothetical CYTOCHROME P450 98A2 (EC 1.14.—.—). TC78082 AW738012 cTOD4P2 XVIIH7 T5O13 R12 C15 r3-c2 r4-c4 GP|2738998|gb|AAB94587.1||AF022458 CYP98A2p {Glycine max}PIR|T0 branched-chain amino acid aminotransferase {Solanum TC78133 AW034300 cLEC37H2 IVD9 T1H18 R7 C8 r1-c2 r3-c3 tuberosum} geranylgeranyl pyrophosphate synthase-related protein TC78147 AI779636 cLES8N7 XIB5 T3D9 R16 C4 r2-c1 r4-c3 {Arabidopsis thaliana}GP|7270829|emb|CAB80510 putative phosphatidylserine decarboxylase {Arabidopsis TC78160 AI776470 cLER18H17 IXH6 T3O11 R14 C15 r2-c1 r4-c3 thaliana}GP|7269448|emb|CAB79452.1||AL161564 cytochrome P450 {Catharanthus TC78161 AW160266 cLPT1K21 XVH9 T4P17 R8 C16 r2-c2 r1-c4 roseus}PIR|T09999|T09999 cytochrome P450- Madagascar periwinkle CYTOCHROME P450 71A9 (EC 1.14.—.—) (P450 TC78170 AI489371 cLED16B17 IIIA7 T1B13 R12 C2 r1-c2 r3-c3 CP1).GP|3334659|emb|CAA71513.1||Y10489 putative cytochrome bA554C12.1 (RBX1 or ROC1 (ring-box or ring finger TC78191 BF114334 cLEY26D17 XXIIA7 T6A14 R11 C1 r3-c1 r2-c4 protein 1)) {Homo sapiens}GP|4769004|gb|AAD29715. alpha amylase precursor {Cuscuta TC78197 BE436573 cLEG33K23 VIB10 T2C20 R5 C3 r4-c2 r1-c3 reflexa}GP|458456|gb|AAA16513.1||U06754 alpha amylase precursor {C putative strictosidine synthase-like {Arabidopsis TC78210 BG629491 cLEL27O9 XXIG10 T6M19 R6 C13 r3-c1 r2-c4 thaliana} malate dehydrogenase, mitochondrial precursor TC78217 BG643772 cTOF32F13 XXC11 T5F22 R3 C6 r3-c2 r4-c4 {Citrullus vulgaris}EGAD|148462|158380 hypothetical p flavanone 3-hydroxylase {Citrus sinensis} TC78218 BG628989 cLEL24M13 XXIF8 T6K15 R12 C11 r3-c1 r2-c4 Contains similarity to gb|Y13720 Hap2a transcription TC78236 BF114407 cLEY26J2 XIVC5 T4E10 R15 C5 r2-c2 r1-c4 factor from Arabidopsis thaliana.PIR|A86430|A8 GALACTOKINASE (EC 2.7.1.6) (GALACTOSE TC78245 AW648708 cLEI5C16 VIIE11 T2J21 R4 C10 r4-c2 r1-c3 KINASE).GP|12322687|gb|AAG51339.1|AC020580_19 AC020580 galact DIACYLGLYCEROL KINASE 1 (EC 2.7.1.107) TC78269 AI489194 cLED17O10 IIIB4 T1D7 R18 C4 r1-c2 r3-c3 (DIGLYCERIDE KINASE) (DGK 1) (DAG KINASE 1).GP|1374772|dbj|B myb-related transcription factor LBM1 {Nicotiana TC78270 AW032347 cLEC35G10 IIB4 T1C8 R17 C3 r1-c2 r3-c3 tabacum} transcription factor {Vicia TC78324 BG127573 cTOF17D4 XIXA12 T5B23 R2 C2 r3-c2 r4-c4 faba}GP|2104679|emb|CAA66480.1||X97906 transcription factor {Vicia faba alpha-glucan phosphorylase, h isozyme phosphorylase TC78327 AW616810 cLHT17D11 XVA4 T4B7 R18 C2 r2-c2 r1-c4 h) {Solanum tuberosum}SP|P32811|PHSH_SOLTU ALPH isocitrate dehydrogenase (NAD+) {Solanum TC78346 AW441655 cLEN17P4 IXB5 T3C9 R16 C3 r2-c1 r4-c3 tuberosum} NADH dehydrogenase (ubiquinone) (EC 1.6.5.3) chain TC78368 AI771898 cLED38E16 IIIH6 T1P11 R14 C16 r1-c2 r3-c3 nad9-wheat mitochondrion Zn finger protein {Nicotiana TC78369 BG130539 cTOF30L15 XXB12 T5D24 R1 C4 r3-c2 r4-c4 tabacum}GP|1360086|emb|CAA66605.1||X97946 Zn finger protein {Nicotiana flavonoid 3′,5′-hydroxylase-like; cytochrome P450 TC78380 AW033148 cLEC25H6 IF9 T1K17 R8 C11 r1-c2 r3-c3 {Arabidopsis thaliana} geranylgeranyl pyrophosphate synthetase precursor TC78381 BE461170 cLEG37B6 VID6 T2G12 R13 C7 r4-c2 r1-c3 (ggpp synthetase) (dimethylallyltransferase {Capsi MYB-like DNA-binding domain protein {Gossypium TC78385 BG123392 cTOF1F20 XIXD2 T5H3 R22 C8 r3-c2 r4-c4 hirsutum}PIR|T09745|T09745 myb-related protein-upl homeobox 2 protein TC78390 AI897000 cLED26E19 IIID8 T1H15 R12 C8 r1-c2 r3-c3 Contains similarity to dTPD-D-glucose-4,6-dehydratase TC78391 BE353784 cTOD6E6 XXIF3 T6K5 R20 C11 r3-c1 r2-c4 from Sphingomonas sp.S88 gb|U51197 and contain fructokinase TC78393 BE433756 cLEG20H18 VG3 T2M5 R20 C13 r4-c2 r1-c3 fructose-6-phosphate 2-kinase/fructose-2,6- TC78403 AW031877 cLEC38I8 IIC8 T1E16 R9 C5 r1-c2 r3-c3 bisphosphatase {Solanum tuberosum}PIR|T07016|T07016 6-ph cytochrome P450 {Nicotiana TC78431 AW034715 cLEC32H2 IH10 T1O19 R6 C15 r1-c2 r3-c3 tabacum}GP|1171579|emb|CAA64635.1||X95342 cytochrome P450 {Nicotiana tab MADS-box transcription factor FBP21 {Petunia x TC78439 AW219022 cLEX2O20 XIIID10 T4G19 R6 C7 r2-c2 r1-c4 hybrida} 76 kDa mitochondrial complex I unit {Solanum TC78448 AW096331 cLET38C16 XXH5 T5P10 R15 C16 r3-c2 r4-c4 tuberosum}SP|Q43644|NUAM_SOLTU NADH- UBIQUINONE OXID contains similarity to SNF2/RAD54 family (RAD26 TC78453 AW647754 cLEI2K21 IVE11 T1J22 R3 C10 r1-c2 r3-c3 family) transcription-repair coupling factor~gene homeodomain protein {Malus x domestica} TC78458 AW033434 cLEC28H13 IG4 T1M7 R18 C13 r1-c2 r3-c3 transcription regulator Sir2-like protein {Arabidopsis TC78492 BF050336 cLEM17M10 VIIH1 T2P1 R24 C16 r4-c2 r1-c3 thaliana}GP|12006420|gb|AAG44850.1|AF283757 pyrophosphate-dependent phosphofructokinase beta TC78498 AW980091 cLEW10K9 XIID3 T3H6 R19 C8 r2-c1 r4-c3 unit {Citrus x paradisi} CYP83D1p {Glycine max}PIR|T05940|T05940 TC78508 BG128761 cTOF22C6 XIXE8 T5J15 R12 C10 r3-c2 r4-c4 cytochrome P450 83D1p-soybean (fragment) Putative UDP-glucose:sterol glucosyltransferase TC78531 BE433289 cLEG13A17 VE2 T2I3 R22 C9 r4-c2 r1-c3 {Arabidopsis thaliana}PIR|D96499|D96499 probable UD contains similarity to cyclopropane fatty acid TC78544 AW399701 cLPT8B18 VB5 T2C9 R16 C3 r4-c2 r1-c3 synthase~gene_id: MEE5.5 {Arabidopsis thaliana} zinc finger and C2 domain protein {Arabidopsis TC78550 AW220607 cLEF1F13 IVE4 T1J8 R17 C10 r1-c2 r3-c3 thaliana} cinnamoyl CoA reductase-like protein {Arabidopsis TC78570 BE433400 cLEG13O12 VE5 T2I9 R16 C9 r4-c2 r1-c3 thaliana}PIR|T48643|T48643 cinnamoyl CoA reductas tyrosine aminotransferase-like protein {Arabidopsis TC78598 AW034806 cLEC32E16 IH9 T1O17 R8 C15 r1-c2 r3-c3 thaliana} omega-3 fatty acid desaturase, endoplasmic reticulum TC78627 BG626797 cLEL14E18 XXIB10 T6C19 R6 C3 r3-c1 r2-c4 {Nicotiana tabacum}SP|P48626|FD3E_TOBAC OMEGA- anthranilate phosphoribosyltransferase-like protein TC78632 AW625356 cLEZ12M21 XIVD3 T4G6 R19 C7 r2-c2 r1-c4 {Arabidopsis thaliana}PIR|T46010|T46010 anthran putative folylpolyglutamate synthetase {Oryza sativa} TC78676 BF050762 cLEM19B11 VIIH4 T2P7 R18 C16 r4-c2 r1-c3 transcription factor IIA large unit {Arabidopsis TC78698 BG140116 cLPP16A16 XVD12 T4H23 R2 C8 r2-c2 r1-c4 thaliana}PIR|T51333|T51333 transcription factor putative alpha-amylase; 60344-64829 {Arabidopsis TC78700 AI775160 cLER14P7 VIIIG9 T2N18 R7 C14 r4-c2 r1-c3 thaliana}PIR|E96720|E96720 probable alpha-amylase polyneuridine aldehyde esterase {Rauvolfia serpentina} TC78712 AW224223 cLEN16B20 IXA7 T3A13 R12 C1 r2-c1 r4-c3 2S seed albumin-1 large unit [Lycopersicon TC78715 AW930900 cLEF42G23 IVF9 T1L18 R7 C12 r1-c2 r3-c3 esculentum] Strong similarity to F19I3.8 GP|3033381 putative UDP- TC78747 BF098180 cLEW26C4 XIIG11 T3N22 R3 C14 r2-c1 r4-c3 galactose-4-epimerase from Arabidopsis thaliana Similar to gb|AF135422 GDP-mannose TC78749 AW218839 cLEX1M19 XIIID7 T4G13 R12 C7 r2-c2 r1-c4 pyrophosphorylase A (GMPPA) from Homo sapiens. ESTs gb|AA712990, heat stress transcription factor 8 TC78884 AW933448 cLEF55G15 VB10 T2C19 R6 C3 r4-c2 r1-c3 pyruvate kinase, cytosolic isozyme {Nicotiana TC78918 BE436523 cLEG33A19 VIB4 T2C8 R17 C3 r4-c2 r1-c3 tabacum}SP|Q42954|KPYC_TOBAC PYRUVATE KINASE, CYTOSOL 2-oxoglutarate/malate translocator precursor-like protein TC78921 BG124992 cTOF7G4 XXF8 T5L16 R9 C12 r3-c2 r4-c4 {Arabidopsis thaliana}PIR|T49900|T49900 2 cytochrome P450 {Solanum tuberosum} TC78950 BG132478 cTOE7P21 XIIE8 T3J16 R9 C10 r2-c1 r4-c3 CYTOCHROME P450 97B2 (EC 1.14.—.—). TC78953 AI482612 cLEB1M6 IA8 T1A15 R12 C1 r1-c2 r3-c3 GP|2738996|gb|AAB94586.1||AF022457 CYP97B2p {Glycine max}PIR|T0 alpha-glucosidase {Solanum TC78967 AW441540 cLEN17F21 IXA12 T3A23 R2 C1 r2-c1 r4-c3 tuberosum}PIR|T07391|T07391 probable alpha- glucosidase (EC 3.2.1.20)-p threonine synthase {Solanum tuberosum} TC78978 AI781552 cLES16I21 XE11 T3I22 R3 C9 r2-c1 r4-c3 NADH dehydrogenase unit TC79000 BG642939 cTOF26I17 XIXH7 T5P13 R12 C16 r3-c22 r4-c4 RING-H2 finger protein RHF2a {Arabidopsis TC79012 AW031373 cLEC40A4 IID3 T1G6 R19 C7 r1-c2 r3-c3 thaliana}GP|13374859|emb|CAC34493.1||AL589883 RING-H2 fin putative C3HC4-type RING zinc finger/ankyrin protein TC79013 BG130531 cTOF30J21 XXB11 T5D22 R3 C4 r3-c2 r4-c4 {Arabidopsis thaliana}PIR|E84689|E84689 probab Dof zinc finger protein {Solanum tuberosum} TC79103 AW033619 cLEC30H5 IH5 T1O9 R16 C15 r1-c2 r3-c3 glucose acyltransferase {Lycopersicon pennellii} TC79131 AI778151 cLES4I7 XH6 T3O12 R13 C15 r2-c2 r4-c3 tyrosine decarboxylase {Arabidopsis thaliana} TC79134 AW029702 cLEC28B17 IG2 T1M3 R22 C13 r1-c2 r3-c3 aldose-1-epimerase-like protein {Nicotiana TC79135 AI778167 cLES4K17 XH7 T3O14 R11 C15 r2-c1 r4-c3 tabacum}PIR|T01933|T01933 probable aldose 1- epimerase (E putative ABC transporter {Arabidopsis TC79147 AW033127 cLEC25J19 IF11 T1K21 R4 C11 r1-c2 r3-c3 thaliana}GP|4115931|gb|AAD03441.1||AF118223 contains similari polyneuridine aldehyde esterase {Rauvolfia serpentina} TC79199 BF097870 cLEW24G19 XIIG6 T3N12 R13 C14 r2-c1 r4-c3 glycogen (starch) synthase precursor {Solanum TC79234 BG128517 cTOF21A12 XIXD12 T5H23 R2 C8 r3-c2 r4-c4 tuberosum}SP|Q00775|UGST_SOLTU GRANULE- BOUND GLYCOGEN alpha glucosidase-like protein {Arabidopsis thaliana} TC79238 BG128749 cTOF21P16 XIXE6 T5J11 R14 C10 r3-c2 r4-c4 transcription factor TEIL {Nicotiana tabacum} TC79239 BE461679 cLEG39L11 VIE8 T2I16 R9 C9 r4-c2 r1-c3 neutral invertase, putative {Arabidopsis TC79243 BE436756 cLEG34I5 VIC3 T2E6 R19 C5 r4-c2 r1-c3 thaliana}GP|12324537|gb|AAG52223.1|AC021665_6|AC021665 put putative alpha-amylase; 60344-64829 {Arabidopsis TC79253 BE460819 cLEG36H15 VIC12 T2E24 R1 C5 r4-c2 r1-c3 thaliana}PIR|E96720|E96720 probable alpha-amylase HOMEOBOX-LEUCINE ZIPPER PROTEIN HAT7 TC79277 AW932596 cLEF49E14 VA2 T2A3 R22 C1 r4-c2 r1-c3 (HD-ZIP PROTEIN 7) (HD-ZIP PROTEIN ATHB- 3).GP|549891|gb|AAA569 Similar to UTP-glucose glucosyltransferases TC79292 AI894979 cLEC6M20 IIE11 T1I22 R3 C9 r1-c2 r3-c3 {Arabidopsis thaliana}PIR|G86144|G86144 hypothetical pr CYP83D1p {Glycine max}PIR|T05940|T05940 TC79302 AI895470 cLEC7L16 IIF2 T1K4 R21 C11 r1-c2 r3-c3 cytochrome P450 83D1p-soybean (fragment) mas-binding factor MBF2 = transcription factor TGA1a TC79327 BF114052 cLEY24E3 XIVC2 T4E4 R21 C5 r2-c2 r1-c4 homolog {Solanum tuberosum = potatoes, root, Peptid cytochrome P450 {Arabidopsis thaliana} TC79360 AI489348 cLED16E20 IIIA9 T1B17 R8 C2 r1-c2 r3-c3 invertase inhibitor homolog {Nicotiana TC79368 BG135878 cTOE23N10 XVIIIE10 T5I20 R5 C9 r3-c2 r4-c4 tabacum}PIR|T03396|T03396 invertase inhibitor homolog-comm putative cytochrome P450 {Arabidopsis TC79382 BE432001 cLEG4D22 VIG11 T2M22 R3 C13 r4-c2 r1-c3 thaliana}GP|13877661|gb|AAK43908.1|AF370589_1|AF370589 putati triosephosphate isomerase, cytosolic {Coptis TC79385 BE431756 cLEG1N4 VG1 T2M22 R3 C13 r4-c2 r1-c3 japonica}SP|P21820|TPIS_COPJA TRIOSEPHOSPHATE ISOMERAS putative ABC transporter; 60211-54925 {Arabidopsis TC79386 AI488143 cLED21K11 IIIC4 T2M1 R24 C13 r4-c2 r1-c3 thaliana}PIR|E96742|E96742 probable ABC transpor tyrosine aminotransferase-like protein {Arabidopsis TC79388 AI487927 cLEN6G15 IXD1 T1F7 R18 C6 r1-c2 r3-c3 thaliana} fructose-6-phosphate 2-kinase/fructose-2,6- TC79403 AW650251 cLEI12O14 VIIB3 T3G1 R24 C7 r2-c1 r4-c3 bisphosphatase {Solanum tuberosum}PIR|T07016|T07016 6-ph putative glycerol-3-phosphate dehydrogenase TC79406 AW650191 cLEI12C14 VIIB1 T2D1 R24 C4 r4-c2 r1-c3 {Arabidopsis thaliana} putative cytochrome P450 {Oryza sativa} TC79461 BE354362 cTOD10I12 XVIIF9 T5K17 R8 C11 r3-c2 r4-c4 cytochrome P450 {Arabidopsis thaliana} TC79463 AW650677 cLEI13B24 VIIB5 T2D9 R16 C4 r4-c2 r1-c3 anthranilate synthase alpha subunit {Catharanthus TC79471 AW651095 cLEI15B17 VIIC5 T2F9 R16 C6 r4-c2 r1-c3 roseus} homeodomain protein {Malus x domestica} TC79485 AW623494 cTOB10J8 XVIF10 T4L20 R5 C12 r2-c2 r1-c4 ferredoxin--nitrite reductase (EC 1.7.7.1) nir-3- TC79488 AW039265 cLET8L21 XIIC12 T3F24 R1 C6 r2-c1 r4-c3 common tobacco (fragment) putative sugar transporter {Arabidopsis thaliana} TC79538 BE458971 cLEM5K9 VIIIE1 T2J2 R23 C10 r4-c2 r1-c3 transcription factor-like protein {Arabidopsis thaliana} TC79544 AW624307 cTOB15C3 XVIH12 T4P24 R1 C16 r2-c2 r1-c4 Similar to UTP-glucose glucosyltransferases TC79554 AW945064 cTOB16E10 XVIIA4 T5A7 R18 C1 r3-c2 r4-c4 {Arabidopsis thaliana}PIR|G86144|G86144 hypothetical pr RING finger protein {Arabidopsis TC79564 AW034559 cLEC24E2 IF5 T1K9 R16 C11 r1-c2 r3-c3 thaliana}GP|4689366|gb|AAD27870.1|AF134155_1|AF134155 RING finger hexokinase TC79603 AW649867 cLEI9L20 VIIG6 T2N11 R14 C14 r4-c2 r1-c3 starch-branching enzyme-like protein {Arabidopsis TC79638 BG130892 cTOE1P21 XVIIID12 T5G24 R1 C7 r3-c2 r4-c4 thaliana} formyltransferase purU homolog {Arabidopsis TC79642 AW944789 cTOB12M15 XVIG12 T4N24 R1 C14 r2-c2 r1-c4 thaliana}GP|2245095|emb|CAB10517.1||Z97343 formyltransf putative heat shock transcription factor {Arabidopsis TC79646 AW930998 cLEF42K16 IVF10 T1L20 R5 C12 r1-c2 r3-c3 thaliana}PIR|T02609|T02609 probable heat shoc Identical to A. thaliana Myb-like protein (gb|D58424). TC79650 BG130692 cTOE1A13 XVIIID7 T5G14 R11 C7 r3-c2 r4-c4 {Arabidopsis thaliana}PIR|F86231|F86231 hypo nucleoside diphosphate kinase {Pisum sativum} TC79659 BG127408 cTOF16M2 XIXA10 T5B19 R6 C2 r3-c2 r4-c4 putative C3HC4-type RING zinc finger/ankyrin protein TC79668 BG131674 cTOE4L22 XVIIIF9 T5K18 R7 C11 r3-c2 r4-c4 {Arabidopsis thaliana}PIR|E84689|E84689 probab isopentenyl diphosphate isomerase 1 {Nicotiana TC79669 BG131971 cTOE5L2 XVIIIF11 T5K22 R3 C11 r3-c2 r4-c4 tabacum} vacuolar ATP synthase catalytic subunit a kDa subunit) TC79686 BG131561 cTOE4F15 XVIIIF7 T5K14 R11 C11 r3-c2 r4-c4 {Daucus carota}SP|P09469|VATA_DAUCA VACUOLAR zinc-finger-like protein {Arabidopsis TC79692 BG132621 cTOE8I16 XVIIIG4 T5M8 R17 C13 r3-c2 r4-c4 thaliana}PIR|T45654|T45654 zinc-finger-like protein- Arabido phaseolin G-box binding protein PG1 {Phaseolus TC79707 AW037806 cLET3D22 XIH8 T3P15 R12 C16 r2-c1 r4-c3 vulgaris}GP|1142619|gb|AAB00686.1||U18348 phaseolin ALTERNATIVE OXIDASE 1 PRECURSOR (EC 1.—.—. TC79757 BE344500 cLEY7C9 XIVC9 T4E18 R7 C5 r2-c2 r1-c4 —).GP|558054|gb|AAC60576.1||S71335 alternative oxidase, A dTDP-glucose 4-6-dehydratase-like protein TC79798 AW035990 cLEC33N6 IIA6 T1A12 R13 C1 r1-c2 r3-c3 {Arabidopsis thaliana}PIR|T45892|T45892 dTDP- glucose 4-6- flavonol 3-o-glucosyltransferase 6 {Manihot TC79809 AI895028 cLEC6H13 IIE7 T1I14 R11 C9 r1-c2 r3-c3 esculenta}SP|Q40288|UFO6_MANES FLAVONOL 3- O-GLUCOSYLTRA soluble starch (bacterial glycogen) synthase {Solanum TC79837 AW929169 cTOC4P12 XVIID12 T5G23 R2 C7 r3-c2 r4-c4 tuberosum}SP|P93568|UGS2_SOLTU SOLUBLE GLYCOG lipoxygenase {Lycopersicon TC79855 AW929070 cTOC4A9 XVIID8 T5G15 R12 C7 r3-c2 r4-c4 esculentum}GP|1654138|gb|AAB65766.1||U37839 lipoxygenase {Lycopersicon e alpha-glucosidase {Solanum TC79865 AW093459 cLET24N10 XIF11 T3L21 R4 C12 r2-c1 r4-c3 tuberosum}PIR|T07391|T07391 probable alpha- glucosidase (EC 3.2.1.20)-p putative tyrosine decarboxylase {Arabidopsis TC79868 BF112371 cLEG41M3 VIF5 T2K10 R15 C11 r4-c2 r1-c3 thaliana}PIR|A84588|A84588 probable tyrosine decarboxy CYTOCHROME P450 83B1 (EC 1.14.—.—). TC79908 AW032343 cLEC35G8 IIB6 T1C12 R13 C3 r1-c2 r3-c3 GP|3164126|dbj|BAA28531.1||D78598 cytochrome P450 monooxygenase lipoxygenase {Solanum TC79919 BF052088 cLEM25F11 VIIIC9 T2F18 R7 C6 r4-c2 r1-c3 tuberosum}GP|1117793|gb|AAD09202.1||U24232 lipoxygenase {Solanum tuberosum}P putative ABC transporter; 73228-76244 {Arabidopsis TC79941 BF113041 cLEG42N24 VIF10 T2K20 R5 C11 r4-c2 r1-c3 thaliana} cytochrome p450 1xxviia2 {Solanum TC79994 AI779493 cLES8M5 XIB3 T3D5 R20 C4 r2-c1 r4-c3 melongena}SP|P37124|C772_SOLME CYTOCHROME P450 77A2 (EC 1.14.—.—) ARF GAP-like zinc finger-containing protein ZiGA4 TC80002 BG137080 cLPP4P19 XVE12 T4J23 R2 C10 r2-c2 r1-c4 (Arabidopsis thaliana} auxin-induced basic helix-loop-helix transcription TC80007 BG125296 cTOF8O13 XXG7 T5N14 R11 C14 r3-c2 r4-c4 factor, putative {Arabidopsis thaliana}GP|123213 contains similarity to limonene TC80009 BG125098 cTOF7L9 XXG1 T5N2 R23 C14 r3-c2 r4-c4 cyclase~gene_id: K15O15.2 {Arabidopsis thaliana} CYTOCHROME P450 90A1 (EC 1.14.—.—). TC80029 BG124599 cTOF5B9 XXE9 T5J18 R7 C10 r3-c2 r4-c4 GP|853719|emb|CAA60793.1||X87367 CYP90 protein {Arabidopsis thal CYTOCHROME P450 84A1 (FERULATE-5- TC80030 BG124625 cTOF5F19 XXE12 T5J24 R1 C10 r3-c2 r4-c4 HYDROXYLASE) (EC 1.14.—.—) (F5H).GP|1488255|gb|AAC49389.1||U38416 transcription factor RUSH-1alpha isolog; 18684-24052 TC80033 AI485822 cLED4C4 XIE9 T3J17 R8 C10 r2-c1 r4-c3 {Arabidopsis thaliana}PIR|A86245|A86245 hypoth FLAVONOID 3′,5′-HYDROXYLASE (EC 1.14.—.—) TC80085 BG134684 cTOE17J5 XVIIID5 T5G10 R15 C7 r3-c2 r4-c4 (F3′5′H) (CYTOCHROME P450 75A4).GP|1620009|dbj|BAA12735.1 76 kDa mitochondrial complex I subunit {Solanum TC80110 AW618774 cLPT16O5 XVHI T4P1 R24 C16 r2-c2 r1-c4 tuberosum}SP|Q43644|NUAM_SOLTU NADH- UBIQUINONE OXID ABC transporter homolog {Populus nigra} TC80115 BF096360 cLEW11G2 XIID6 T3H12 R13 C8 r2-c1 r4-c3 Contains similarity to 12S seed storage globulin TC80151 BG127001 cTOF14G15 XXIB2 T6C3 R22 C3 r3-c1 r2-c4 precursor GP|134919. ESTs gb|T13642, gb|T21684 and decarboxylase like protein {Arabidopsis TC80187 AW038810 cLET5H11 XIIB8 T3D16 R9 C4 r2-c1 r4-c3 thaliana}GP|2245025|emb|CAB10445.1||Z97341 decarboxylase li aldose-1-epimerase-like protein {Nicotiana TC80210 AW041617 cLET9L20 XIID2 T3H4 R21 C8 r2-c1 r4-c3 tabacum}PIR|T01933|T01933 probable aldose 1- epimerase (E ATP synthase alpha subunit, mitochondrial {Nicotiana TC80243 BE436279 cLEG31G12 VIA6 T2A12 R13 C1 r4-c2 r1-c3 plumbaginifolia}SP|P05495|ATP0_NICPL ATP SYNTH cytochrome p450 1xxia2 {Solanum TC80252 AI896171 cLEC14E8 ID4 T1G7 R18 C7 r1-c2 r3-c3 melongena}SP|P37118|C712_SOLME CYTOCHROME P450 71A2 (EC 1.14.—.—) ( CYTOCHROME P450 71A22 (EC 1.14.—.—). TC80253 AI896229 cLEC14O18 ID5 T1G9 R16 C7 r1-c2 r3-c3 GP|4678357|emb|CAB41167.1||AL049659 cytochrome P450-like protei putative dehydroquinase shikimate dehydrogenase TC80290 AW443373 cLET43P18 XIIA8 T3B16 R9 C2 r2-c1 r4-c3 {Arabidopsis thaliana} homogentisate 1,2-dioxygenase {Lycopersicon TC80293 AW160297 cLPT1O3 XVIA1 T4B2 R23 C2 r2-c2 r1-c4 esculentum} general negative transcription regulator-like TC80302 AW398527 cLPT2M6 XVIA5 T4B10 R15 C2 r2-c2 r1-c4 {Arabidopsis thaliana} putative transcriptional co-activator {Arabidopsis TC80320 AW040559 cLET7I18 XIIC3 T3F6 R19 C6 r2-c1 r4-c3 thaliana}GP|3513735|gb|AAC33951.1||AF080118 cont putative cytochrome P450 TC80358 AI782844 cLES20P12 XG11 T3M22 R3 C13 r2-c1 r4-c3 phospho-2-dehydro-3-deoxyheptonate aldolase TC80361 AW738073 cTOD5K17 XXIIA3 T6A6 R19 C1 r3-c1 r2-c4 glyceraldehyde 3-phosphate dehydrogenase a precursor, TC80364 AW039138 cLET8H23 XIIC10 T3F20 R5 C6 r2-c1 r4-c3 chloroplast {Nicotiana tabacum}SP|P09043|G3PA aminomethyltransferase precursor system t protein) TC80365 AW040935 cLET7O18 XIIC6 T3F12 R13 C6 r2-c1 r4-c3 {Solanum tuberosum}SP|P54260|GCST_SOLTU AMINOMET glyceraldehyde 3-phosphate dehydrogenase a precursor, TC80366 BE459022 cLEM5E2 VIIID11 T2H22 R3 C8 r4-c2 r1-c3 chloroplast {Nicotiana tabacum}SP|P09043|G3PA hydroxymethyltransferase {Arabidopsis TC80391 AW219880 cLEX6G15 XIIA7 T3B14 R11 C2 r2-c1 r4-c3 thaliana}GP|2244749|emb|CAB10172.1||Z97335 hydroxymethyltrans hydroxymethyltransferase {Arabidopsis TC80394 BG123319 cTOF1F23 XIXD3 T5H5 R20 C8 r3-c2 r4-c4 thaliana}GP|2244749|emb|CAB10172.1||Z97335 hydroxymethyltrans putative fructose-bisphosphate aldolase, plastidic form TC80401 AI777043 cLEC1C17 IE1 T1I1 R24 C9 r1-c2 r3-c3 {Arabidopsis thaliana}GP|11762176|gb|AAG403 ATP synthase delta' subunit, mitochondrial precursor TC80407 BG125855 cTOF10I1 XVIIIG6 T5M12 R13 C13 r3-c2 r4-c4 {Ipomoea batatas}SP|Q40089|ATP4_IPOBA ATP SYNT glyceraldehyde 3-phosphate dehydrogenase TC80408 BF098524 cLEW27D4 XIIA5 T3B10 R15 C2 r2-c1 r4-c3 S-adenosyl-L-methionine synthetase TC80422 AW038211 cLET1P4 IVE8 T1J16 R9 C10 r1-c2 r3-c3 S-adenosyl-L-methionine synthetase TC80423 BG126068 cTOF10L8 XVIIIG9 T5M18 R7 C13 r3-c2 r4-c4 S-adenosylmethionine synthase 3 {Lycopersicon TC80424 BG130132 cTOF29K10 XXB1 T5D2 R23 C4 r3-c2 r4-c4 esculentum}SP|P43282|METM_LYCES S- ADENOSYLMETHIONINE cystathionine gamma-synthase isoform 1 {Solanum TC80427 AW738500 cTOD7D11 XVID5 T4H10 R15 C8 r2-c2 r1-c4 tuberosum} acetyl-CoA acyltransferase {Cucumis TC80431 AW621464 cLEX12E11 VA6 T2A11 R14 C1 r4-c2 r1-c3 sativus}GP|393707|emb|CAA47926.1||X67696 acetyl- CoA acyltransf xylose isomerase {Hordeum TC80432 AW034312 cLEC33C6 XVIG4 T4N8 R17 C14 r2-c2 r1-c4 vulgare}SP|Q40082|XYLA_HORVU XYLOSE ISOMERASE (EC 5.3.1.5).GP|1296809|em cytochrome P450 {Arabidopsis thaliana} TC80453 BE436610 cLEG33D21 VIB6 T2C12 R13 C3 r4-c2 r1-c3 Contains a PF|00175 Oxidoreductase FAD/NADH- TC80456 AI781810 cLES17M15 XF5 T3K10 R15 C11 r2-c1 r4-c3 binding domain. ESTs:gb|H76345 and gb|AA651465 come fro caffeoyl-coenzymeA O-methyltransferase {Nicotiana TC80468 AI484326 cLES1I19 XG4 T3M8 R17 C13 r2-c1 r4-c3 tabacum}GP|1574946|gb|AAC49913.1||U38612 caffeoyl homologous to GATA-binding transcription factors TC80486 AW030365 cLEC20O14 IE6 T1I11 R14 C9 r1-c2 r3-c3 {Arabidopsis thaliana}GP|7288001|emb|CAB81839.1||A NADP-malic enzyme{circumflex over ( )}{circumflex over ( )}malate dehydrogenase TC80499 AW616575 cLHT11B24 XIVH1 T4O2 R23 C15 r2-c2 r1-c4 MADS box transcription factor-like {Arabidopsis TC80500 BE431840 cLEG4G17 XXIB5 T6C9 R16 C3 r3-c1 r2-c4 thaliana} triosephosphate isomerase, cytosolic {Petunia TC80531 BE433931 cLEG9A4 XVIF4 T4L8 R17 C12 r2-c2 r1-c4 hybrida}SP|P48495|TPIS_PETHY TRIOSEPHOSPHATE ISOMERAS putative homeodomain transcription factor {Arabidopsis TC80540 AI771596 cLED30M20 IIIF9 T1L17 R8 C12 r1-c2 r3-c3 thaliana}PIR|H84774|H84774 probable homeodom malate dehydrogenase {Nicotiana tabacum} TC80550 BF051399 cLET13A12 VIIIB2 T2D4 R21 C4 r4-c2 r1-c3 bZIP DNA-binding protein TC80553 BE460942 cLEG37C1 VID7 T2G14 R11 C7 r4-c2 r1-c3 lysine-ketoglutarate reductase/saccharopine TC80556 AI486763 cLED11B18 IIG7 T1M14 R11 C13 r1-c2 r3-c3 dehydrogenase bifunctional enzyme {Arabidopsis thaliana} phosphoglycerate kinase precursor {Solanum TC80567 BE353948 cTOD8H1 XXH1 T5P2 R23 C16 r3-c2 r4-c4 tuberosum}PIR|T07014|T07014 phosphoglycerate kinase (EC proton pump interactor {Arabidopsis TC80570 AI780385 cLES11L9 XD4 T3G8 R17 C7 r2-c1 r4-c3 thaliana}GP|7269604|emb|CAB81400.1||AL161571 proton pump intera malate dehydrogenase {Glycine max} TC80572 AW039846 cLET13N23 XIC12 T3F23 R2 C6 r2-c1 r4-c3 NADH-ubiquinone oxidoreductase 20 kDa subunit TC80576 AI489373 cLED16D1 IIIA8 T1B15 R12 C2 r1-c2 r3-c3 precursor {Solanum tuberosum}SP|Q43844|NUKM_SOLTU NAD MADS-box transcription factor FBP5 {Petunia x TC80582 AI487071 cLED9G21 IVC11 T1F22 R3 C6 r1-c2 r3-c3 hybrida} serine hydroxymethyltransferase, mitochondrial TC80593 AW092318 cLET19D5 XXID5 T6G9 R16 C7 r3-c1 r2-c4 precursor {Solanum tuberosum}SP|P50433|GLYM_SOLTU SE serine hydroxymethyltransferase, mitochondrial TC80594 AI773651 cLER7B24 XVIA12 T4B24 R1 C2 r2-c2 r1-c4 precursor {Solanum tuberosum}SP|P50433|GLYM_SOLTU SE homeodomain protein TC80595 BG124777 cTOF6M4 XXF4 T5L8 R17 C12 r3-c2 r4-c4 homeodomain leucine-zipper protein ATHB13 TC80599 AI898456 cLED34E15 IIIG5 T1N9 R16 C14 r1-c2 r3-c3 {Arabidopsis thaliana}GP|12325190|gb|AAG52541.1|AC013289 spermidine synthase {Arabidopsis thaliana} TC80606 AW441877 cLEN18F20 XXIB12 T6C23 R2 C3 r3-c1 r2-c4 putative ATP synthase {Arabidopsis TC80612 BG130784 cTOE1C12 XVIIID8 T5G16 R9 C7 r3-c2 r4-c4 thaliana}PIR|B84606|B84606 probable ATP synthase [imported]-Ar dTDP-glucose 4-6-dehydratases-like protein TC80616 AW625812 cLEZ16P14 XIVE3 T4I6 R19 C9 r2-c2 r1-c4 {Arabidopsis thaliana}PIR|T45701|T45701 dTDP- glucose 4-6 homology to pyroxidal-5′-phosphate-dependant TC80620 BE433185 cLEG12J17 IVH8 T1P16 R9 C16 r1-c2 r3-c3 glutamate decarboxylases; putative start codon glutamate decarboxylase {Lycopersicon TC80621 BE434187 cLEG15D21 VE6 T2I11 R14 C9 r4-c2 r1-c3 esculentum}SP|P54767|DCE_LYCES GLUTAMATE DECARBOXYLASE (EC 4. osmotic stress-induced zinc-finger protein {Nicotiana TC80630 AW219530 cLEX4M2 XIIIE8 T4I15 R12 C9 r2-c2 r1-c4 tabacum}PIR|T01985|T01985 zinc-finger protein ferritin subunit cowpea2 precursor {Vigna TC80669 BG129323 cTOF24A17 XIXG5 T5N9 R16 C14 r3-c2 r4-c4 unguiculata}PIR|T08124|T08124 ferritin 2 precursor- cowp contains similarity to NADH dehydrogenase chain CI- TC80670 AW219844 cLEX6E3 XIIIE10 T4I19 R6 C9 r2-c2 r1-c4 18~gene_id: K9I9.16 {Arabidopsis thaliana} succinate dehydrogenase TC80679 BE432138 cLEG6G20 XXIG12 T6M23 R2 C13 r3-c1 r2-c4 putative glycine decarboxylase p-protein TC80681 BE459806 cLEM8I5 XXIG2 T6M3 R22 C13 r3-c1 r2-c4 S-ADENOSYLMETHIONINE DECARBOXYLASE TC80692 AI781600 cLES16D11 XE7 T3I14 R11 C9 r2-c1 r4-c3 PROENZYME (EC 4.1.1.50) (ADOMETDC) (SAMDC).GP|1498080|gb|AAC0461 CONSTANS-like protein 2 {Malus x domestica} TC80693 AI771970 cLER1E6 XA4 T3A8 R17 C1 r2-c1 r4-c3 pyruvate kinase (EC 2.7.1.40), cytosolic-potato TC80694 AW650674 cLEI13B16 VIIB4 T2D7 R18 C4 r4-c2 r1-c3 ATP synthase delta subunit, mitochondrial precursor TC80699 AW625595 cLEZ15N21 XIVD7 T4G14 R11 C7 r2-c2 r1-c4 (oligomycin sensitivity conferral protein) (oscp Tetrafunctional protein of glyoxysomal fatty acid beta- TC80702 BE461193 cLEG37F20 XXID8 T6G15 R12 C7 r3-c1 r2-c4 oxidation {Brassica napus}PIR|T08017|T08017 PROBABLE VACUOLAR ATP SYNTHASE TC80710 AI490156 cLER1C17 XA2 T3A4 R21 C1 r2-c1 r4-c3 SUBUNIT H (EC 3.6.1.34) (V-ATPASE H SUBUNIT) (VACUOLAR PROTON PUMP H Strong similarity to gb|L34684 inosine monophosphate TC80721 AW621167 cLEX11C19 XIIIA12 T4A23 R2 C1 r2-c2 r1-c4 dehydrogenase (IMPDH) from Arabidopsis thaliana phosphate/phosphoenolpyruvate translocator-like TC80730 BG138135 cLPP8K20 XXIF12 T6K23 R2 C11 r3-c1 r2-c4 protein {Arabidopsis thaliana} 3-isopropylmalate dehydrogenase precursor TC80800 BF176554 cLEZ20F11 XXIC9 T6E17 R8 C5 r3-c1 r2-c4 dehydrogenase) (imdh) (3-ipm-dh) {Solanum tuberosum}SP|P2 sucrose transporter TC80801 AW218181 cLEZ1K7 XIVF8 T4K16 R9 C11 r2-c2 r1-c4 citrate synthase, glyoxysomal precursor {Cucurbita TC80803 AW032595 cLEC16J7 XXIA6 T6A11 R14 C1 r3-c1 r2-c4 maxima}SP|P49299|CYSZ_CUCMA CITRATE SYNTHASE, GL UDP-glucose:protein transglucosylase {Solanum TC80818 BF097146 cLEW19H11 XIIE5 T3J10 R15 C10 r2-c1 r4-c3 tuberosum} delta-12 fatty acid desaturase {Borago officinalis} TC80824 AW618696 cLPT14B17 XVG5 T4N9 R16 C14 r2-c2 r1-c4 enoyl-ACP reductase {Petunia x hybrida} TC80834 BF096267 cLEW11G11 XXIA9 T6A17 R8 C1 r3-c1 r2-c4 Similar to acyl carrier protein, mitochondrial precursor TC80836 BF176381 cLEZ20E22 XXIC7 T6E13 R12 C5 r3-c1 r2-c4 (ACP) NADH-ubiquinone oxidoreductase 9.6 KD omega-3 fatty acid desaturase, endoplasmic reticulum TC80843 BG139666 cLPP13J11 XVD7 T4H13 R12 C8 r2-c2 r1-c4 {Nicotiana tabacum}SP|P48626|FD3E_TOBAC OMEGA- UDP-glucose glucosyltransferase {Arabidopsis TC80847 AW035637 cLEC39F24 IIC12 T1E24 R1 C5 r1-c2 r3-c3 thaliana}GP|9392679|gb|AAF87256.1|AC068562_3|AC068562 isocitrate dehydrogenase (NADP+) {Solanum TC80851 AI778998 cLES6F20 XIA3 T3B5 R20 C2 r2-c1 r4-c3 tuberosum}PIR|T07402|T07402 probable isocitrate dehydroge zinc finger protein {Pisum sativum}PIR|T48868|T48868 TC80860 BG138281 cLPP8P2 XVF4 T4L7 R18 C12 r2-c2 r1-c4 zinc finger protein [imported]-garden pea putative ABC transporter ATPase; 10053-12032 TC80867 AW625248 cLEZ13O13 XIVD5 T4G10 R15 C7 r2-c2 r1-c4 {Arabidopsis thaliana} transcriptional regulator, putative; 35498-34111 TC80874 BF051020 cLEM21G18 VC1 T2E1 R24 C5 r4-c2 r1-c3 {Arabidopsis thaliana}PIR|H96576|H96576 hypothetic legumin-like protein {Arabidopsis TC80885 AW224340 cLEN16H12 XIVB5 T4C10 R15 C3 r2-c2 r1-c4 thaliana}PIR|H84687|H84687 legumin-like protein [imported]-Arab ATP:citrate lyase {Capsicum annuum} TC80889 AI488015 cLED19E8 IIIB10 T1D19 R6 C4 r1-c2 r3-c3 hyoscyamine 6-dioxygenase hydroxylase) {Hyoscyamus TC80893 AW650608 cLEI13D23 VIIB8 T2D15 R12 C4 r4-c2 r1-c3 niger}SP|P24397|HY6H_HYONI HYOSCYAMINE 6- DIOXYGE RING-H2 finger protein RHF2a {Arabidopsis TC80911 BE433031 cLEG11N19 XIIIA1 T4A1 R24 C1 r2-c2 r1-c4 thaliana}GP|13374859|emb|CAC34493.1||AL589883 RING-H2 fin putative GDP-mannose pyrophosphorylase; 64911-67597 TC80933 AI898042 cLED31D19 IIIF10 T1L19 R6 C12 r1-c2 r3-c3 {Arabidopsis thaliana}PIR|G96778|G96778 hypothe glucosyltransferase-like protein {Arabidopsis thaliana} TC80941 AI895094 cLEC6D16 IIE5 T1I10 R15 C9 r1-c2 r3-c3 putative caffeoyl-CoA O-methyltransferase TC80956 BE459901 cLEM8I18 XVIE1 T4J2 R23 C10 r2-c2 r1-c4 {Arabidopsis thaliana} fatty acid elongase-like protein (cer2-like) {Arabidopsis TC80962 AW616717 cLHT12O23 XVA3 T4B5 R20 C2 r2-c2 r1-c4 thaliana}GP|7268088|emb|CAB78426.1||AL161 TOM (target of myb1)-like protein {Arabidopsis TC80976 AW616128 cLHT6E15 XVC10 T4F19 R6 C6 r2-c2 r1-c4 thaliana}PIR|T51543|T51543 TOM (target of myb1)- like heat shock transcription factor-like protein {Arabidopsis TC80978 AW223910 cLEN14G3 IXA2 T3A3 R22 C1 r2-c1 r4-c3 thaliana} Similar to ATP-citrate-lyase {Arabidopsis TC80979 BE450968 cLEY15N12 XIIIH7 T4O13 R12 C15 r2-c2 r1-c4 thaliana}PIR|F86227|F86227 hypothetical protein [imported putative NADH-ubiquinone oxireductase {Arabidopsis TC80984 AI772183 cLER1N12 XA10 T3A20 R5 C1 r2-c1 r4-c3 thaliana}PIR|C84588|C84588 probable NADH-ubiquin putative deoxycytidylate deaminase {Cicer arietinum} TC80988 AI774647 cLER12P6 IXE10 T3I19 R6 C9 r2-c1 r4-c3 putative RING finger protein; 84236-82024 TC81001 AW223819 cLEN13D4 VIIIH3 T2P6 R19 C16 r4-c2 r1-c3 {Arabidopsis thaliana}PIR|A96829|A96829 probable RING fin putative RING finger protein; 84236-82024 TC81002 BG126984 cTOF14E5 XIXA3 T5B5 R20 C2 r3-c2 r4-c4 {Arabidopsis thaliana}PIR|A96829|A96829 probable RING fin RING finger-like protein {Arabidopsis TC81013 AW035087 cLEC13K19 IC12 T1E23 R2 C5 r1-c2 r3-c3 thaliana}PIR|T47595|T47595 RING finger protein T12E18.50-Ar mevalonate diphosphate decarboxylase {Arabidopsis TC81015 AW443810 cTOF7H21 XIIB2 T3D4 R21 C4 r2-c1 r4-c3 thaliana}GP|3250736|emb|CAA76803.1||Y17593 mevalo aspartate aminotransferase {Oryza TC81020 BG134029 cTOE15G21 XXIF7 T6K13 R12 C11 r3-c1 r2-c4 sativa}PIR|JC5125|JC5125 aspartate transaminase (EC 2.6.1.1) prec NADP-dependent isocitrate dehydrogenase-like protein TC81025 BG130056 cTOF29M15 XXB3 T5D4 R21 C4 r3-c2 r4-c4 Strong similarity to F19I3.8 GP|3033381 putative UDP- TC81034 BE460513 cLEG31L11 VIA10 T2A20 R5 C1 r4-c2 r1-c3 galactose-4-epimerase from Arabidopsis thaliana glucosyltransferase-like protein {Arabidopsis thaliana} TC81042 AW220225 cLEX9F14 XVIIF3 T5K5 R20 C11 r3-c2 r4-c4 omega-6 fatty acid desaturase, chloroplast precursor TC81045 AI773855 cLER8K22 XC8 T3E16 R9 C5 r2-c1 r4-c3 {Brassica napus}SP|P48627|FD6C_BRANA OMEGA-6 F acyl-ACP thioesterase {Garcinia mangostana} TC81091 AI778618 cLES5J24 XH11 T3O22 R3 C15 r2-c1 r4-c3 ATP synthase a subunit precursor {Nicotiana TC81098 AI483512 cLED25C6 IIID3 T1H5 R20 C8 r1-c2 r3-c3 tabacum}SP|P06288|ATPI_TOBAC ATP SYNTHASE A CHAIN PRECU 3-isopropylmalate dehydrogenase precursor TC81104 AW455243 cLEX10G16 XIIIA7 T4A13 R12 C1 r2-c2 r1-c4 dehydrogenase) (imdh) (3-ipm-dh) {Brassica napus}SP|P2910 anthranilate N-benzoyltransferase {Arabidopsis TC81105 AW030112 cLEC20N19 IE5 T1I9 R16 C9 r1-c2 r3-c3 thaliana} cytochrome c oxidase subunit Vb precursor-like protein TC81111 AI776318 cLER18I21 IXH7 T3O13 R12 C15 r2-c1 r4-c3 {Arabidopsis thaliana} UMP synthase {Nicotiana plumbaginifolia} TC81117 AW626116 cLEZ18K8 XIVE12 T4I24 R1 C9 r2-c2 r1-c4 anthocyanin 5-O-glucosyltransferase {Petunia x TC81118 BE449685 cLEY11E5 XIIIF11 T4K21 R4 C11 r2-c2 r1-c4 hybrida} uridine kinase-like protein {Arabidopsis thaliana} TC81123 AW929478 cTOC9E1 XVIIF5 T5K9 R16 C11 r3-c2 r4-c4 putative homeodomain transcription factor {Arabidopsis TC81124 AW093664 cLET25B16 XIG1 T3N1 R24 C14 r2-c1 r4-c3 thaliana}PIR|H84774|H84774 probable homeodom glucose-regulated protein 78 TC81129 AW040053 cLET19M12 XIE2 T3J3 R22 C10 r2-c1 r4-c3 contains similarity to acyl-CoA TC81143 BE450029 cLEY11D6 XIIIF10 T4K19 R6 C11 r2-c2 r1-c4 thioesterase~gene_id: K23F3.9 {Arabidopsis thaliana} HOMEOBOX-LEUCINE ZIPPER PROTEIN HAT5 TC81154 AW220361 cLEX10P11 XIIIA11 T4A21 R4 C1 r2-c2 r1-c4 (HD-ZIP PROTEIN 5) (HD-ZIP PROTEIN ATHB- 1).□GP|16329|emb|CAA416 phosphoenolpyruvate carboxylase 1 {Gossypium TC81155 AW223731 cLEN12P6 VIIIH1 T2P2 R23 C16 r4-c2 r1-c3 hirsutum}GP|2266947|gb|AAB80714.1||AF008939 phosphoeno transcription factor CRC {Arabidopsis TC81170 AI489150 cLED15E7 IIIA2 T1B3 R22 C2 r1-c2 r3-c3 thaliana}GP|12325076|gb|AAG52485.1|AC018364_3|AC018364 transc putative glucose regulated repressor protein TC81176 AW617956 cLPT11F3 XVF10 T4L19 R6 C12 r2-c2 r1-c4 {Arabidopsis thaliana}PIR|A84649|A84649 probable gluco cytochrome P450 {Nicotiana TC81178 BF051289 cLEM22K1 VIIIB3 T2D6 R19 C4 r4-c2 r1-c3 tabacum}GP|1237250|emb|CAA65580.1||X96784 cytochrome P450 {Nicotiana tab tryptophan synthase alpha 1-like protein {Arabidopsis TC81185 BG643947 cTOF33J9 XXD4 T5H6 R19 C8 r3-c2 r4-c4 thaliana}GP|3892048|gb|AAC78257.1|AAC78257|AC small zinc finger-like protein TC81193 BG129576 cTOF25A17 XIXG9 T5N17 R8 C14 r3-c2 r4-c4 MybSt1 {Solanum tuberosum} TC81223 AI484070 cLED22J14 IIIC7 T1F13 R12 C6 r1-c2 r3-c3 immediate-early salicylate-induced glucosyltransferase TC81244 AW441527 cLEN17D17 IXA10 T3A19 R6 C1 r2-c1 r4-c3 {Nicotiana tabacum}GP|1685005|gb|AAB36653.1| bZIP transcription factor {Nicotiana tabacum} TC81272 BG124528 cTOF5H16 XIH10 T3P19 R6 C16 r2-c1 r4-c3 aspartate aminotransferase, cytoplasmic {Daucus TC81279 BG123545 cTOF2C6 XXB5 T5D10 R15 C4 r3-c2 r4-c4 carota}SP|P28734|AATC_DAUCA ASPARTATE AMINOTRANSFER putative RING zinc finger protein; 53384-54880 TC81280 AW455343 cLEX10C4 XIIIA6 T4A11 R14 C1 r2-c2 r1-c4 {Arabidopsis thaliana}PIR|G96835|G96835 probable RIN similar to ATPases associated with various cellular TC81288 AW033821 cLEC29N4 IG12 T1M23 R2 C13 r1-c2 r3-c3 activites (Pfam: AAA.hmm, score: 230.91) {Arabid ASPARTATE AMINOTRANSFERASE, TC81293 AI486001 cLED3P14 XXIB7 T6C13 R12 C3 r3-c1 r2-c4 MITOCHONDRIAL PRECURSOR (EC 2.6.1.1) (TRANSAMINASE A).GP|531555|emb|CAA phosphoribosylanthranilate transferase {Arabidopsis TC81302 BE459246 cLEM6A14 VB7 T2C13 R12 C3 r4-c2 r1-c3 thaliana} D-ribulose-5-phosphate 3-epimerase {Oryza sativa} TC81304 AI896020 cLEC13J3 IC10 T1E19 R6 C5 r1-c2 r3-c3 malate dehydrogenase, glyoxysomal precursor TC81324 AW222290 cLEN7H3 IXD6 T3G11 R14 C7 r2-c1 r4-c3 {Citrullus vulgaris}EGAD|130842|139627 glyoxysomal mala glyceraldehyde 3-phosphate dehydrogenase, cytosolic TC81336 BG127844 cTOF18C20 XIXB9 T5D17 R8 C4 r3-c2 r4-c4 {Petunia hybrida}SP|P26520|G3PC_PETHY GLYCERALD CCAAT-binding transcription factor subunit A(CBF-A) TC81341 AI780026 cLES9N8 XIB10 T3D19 R6 C4 r2-c1 r4-c3 {Arabidopsis thaliana}GP|2244810|emb|CAB10233.1 H+-transporting ATPase-like protein {Arabidopsis TC81342 AW038933 cLET10I17 XXIF9 T6K17 R8 C11 r3-c1 r2-c4 thaliana}GP|7270157|emb|CAB79970.1||AL161581 H+- tr ZF-ED homeobox protein {Flaveria bidentis} TC81347 BG125944 cTOF10O6 XVIIIG10 T5M20 R5 C13 r3-c2 r4-c4 PUTATIVE NADH-UBIQUINONE TC81349 BG643035 cTOF26K20 XXIC11 T6E21 R4 C5 r3-c1 r2-c4 OXIDOREDUCTASE SUBUNIT B17.2 (EC 1.6.5.3) (EC 1.6.99.3) (COMPLEX I-B17.2) ( SNF5, transcription regulatory protein homolog BSH TC81352 AI894835 cLEC6E3 XXIH2 T6O3 R22 C15 r3-c1 r2-c4 {Arabidopsis thaliana} putative glucosyltransferase {Arabidopsis TC81356 BE436042 cLEG30F1 VIA2 T2A4 R21 C1 r4-c2 r1-c3 thaliana}GP|4309698|gb|AAD15482.1||AC006266 putative gluc glutamine cyclotransferase precursor {Carica TC81367 BE459845 cLEM8O15 VIIIF10 T2L20 R5 C12 r4-c2 r1-c3 papaya}PIR|T08168|T08168 glutaminyl-peptide cyclotrans contains similarity to sugar transporters (Pfam: TC81373 AW737195 cTOD2G24 XXIA3 T6A5 R20 C1 r3-c1 r2-c4 sugar_tr.hmm, score: 395.91) {Arabidopsis thaliana} putative folylpolyglutamate synthetase {Oryza sativa} TC81390 AW033669 cLEC30B12 IH3 T1O5 R20 C15 r1-c2 r3-c3 S-adenosyl-L-methionine Mg-protoporphyrin IX TC81391 BG128901 cTOF22P13 XIXF3 T5L5 R20 C12 r3-c2 r4-c4 methyltranserase {Nicotiana tabacum} contains similarity to ATP synthase B/B′ (Pfam: ATP- TC81399 AW223278 cLEN11G3 VIIIG5 T2N10 R15 C14 r4-c2 r1-c3 synt_B.hmm, score: 11.71) {Arabidopsis thaliana} Contains similarity to gb|AJ006354 zinc finger protein TC81419 AW441698 cLEN18K1 IXB8 T3C15 R12 C3 r2-c1 r4-c3 (ZAC) from Homo sapiens. {Arabidopsis thalian dihydroflavonol 4-reductase-like {Arabidopsis thaliana} TC81435 AW622813 cTOB1M3 XVIIB1 T5C1 R24 C3 r3-c2 r4-c4 putative RING zinc finger protein {Arabidopsis TC81454 AI488569 cLED17F6 IIIB2 T1D3 R22 C4 r1-c2 r3-c3 thaliana} beta-amylase {Arabidopsis thaliana} TC81481 BG135937 cLPP1I15 XVE5 T4J9 R16 C10 r2-c2 r1-c4 zinc finger-like protein {Arabidopsis TC81513 BG134694 cTOE17L7 XXH4 T5P8 R17 C16 r3-c2 r4-c4 thaliana}PIR|T49033|T49033 zinc finger-like protein- Arabido putative methylmalonate-semi-aldehyde dehydrogenase TC81537 AW649038 cLEI6J14 VIIF5 T2L9 R16 C12 r4-c2 r1-c3 {Arabidopsis thaliana}PIR|H84514|H84514 hypothe myb-related protein 340-garden snapdragon TC81538 AI486576 cLED6E18 IVB6 T1D12 R13 C4 r1-c2 r3-c3 ISOCITRATE DEHYDROGENASE [NADP] (EC TC81566 AW094166 cLET27B21 XIG5 T3N9 R16 C14 r2-c1 r4-c3 1.1.1.42) (OXALOSUCCINATE DECARBOXYLASE) (IDH) (NADP+-SPECIFIC I UTP-glucose glucosyltransferase-like protein TC81577 AW649171 cLEI7I4 VIIF12 T2L23 R2 C12 r4-c2 r1-c3 {Arabidopsis thaliana}GP|4835225|emb|CAB42903.1||AL049 flavanone 3beta-hydroxylase {Petunia x hybrida} TC81579 BE462481 cTOA13M9 XVID7 T4H14 R11 C8 r2-c2 r1-c4 pyruvate kinase {Arabidopsis thaliana} TC81587 BG134368 cTOE16K9 XVIIIC12 T5E24 R1 C5 r3-c2 r4-c4 serine hydroxymethyltransferase, mitochondrial TC81590 BE432582 cLEG8L10 VIH11 T2O22 R3 C15 r4-c2 r1-c3 precursor {Solanum tuberosum}SP|P50433|GLYM_SOLTU SE serine hydroxymethyltransferase, mitochondrial TC81591 BE460493 cLEG31H1 VIA7 T2A14 R11 C1 r4-c2 r1-c3 precursor {Solanum tuberosum}SP|P50433|GLYM_SOLTU SE biotin carboxylase subunit {Nicotiana TC81634 AW222488 cLEN8G14 IVD4 T1H8 R17 C8 r1-c2 r3-c3 tabacum}GP|870726|gb|AAC41659.1||L38260 biotin carboxylase su ornithine carbamoyltransferase {Pisum TC81652 BG125394 cTOF8B19 XXG3 T5N6 R19 C14 r3-c2 r4-c4 sativum}SP|Q43814|OTC_PEA ORNITHINE CARBAMOYLTRANSFERASE PREC phosphoenolpyruvate carboxylase kinase {Lycopersicon TC81676 AW223421 cLEN11J18 VIIIG7 T2N14 R11 C14 r4-c2 r1-c3 esculentum} UDP-glucose glucosyltransferase {Solanum TC81688 BG133854 cTOE14G24 XVIF6 T4L12 R13 C12 r2-c2 r1-c4 tuberosum}GP|1857447|gb|AAB48444.1||U82367 UDP- glucose glu Strong similarity to UDP-glucose glucosyltransferase TC81690 AW033693 cLEC29O17 IH1 T1O1 R24 C15 r1-c2 r3-c3 from Arabidopsis thaliana gb|AB016819 and conta transcription factor NF-Y, CCAAT-binding-like protein TC81698 AW621652 cLEX12N12 XIIIB11 T4C21 R4 C3 r2-c2 r1-c4 {Arabidopsis thaliana}PIR|T45874|T45874 trans malate dehydrogenase (NADP), chloroplast precursor TC81700 BE458361 cLEM1J8 XIXA6 T5B11 R14 C2 r3-c2 r4-c4 (NADp-mdh) {Pisum sativum}SP|P21528|MDHC_PEA MAL acyl-CoA:1-acylglycerol-3-phosphate acyltransferase TC81716 BE353669 cTOA19N6 XVIE7 T4J14 R11 C10 r2-c2 r1-c4 {Arabidopsis thaliana} VACUOLAR ATP SYNTHASE SUBUNIT G 2 (EC TC81726 AW094576 cLET29A14 XIG8 T3N15 R12 C14 r2-c1 r4-c3 3.6.1.34) (V-ATPASE G SUBUNIT 2) (VACUOLAR PROTON PUMP G SUBUN MADS-box transcription factor jointless TC81749 AI489275 cLED17L17 IIIB3 T1D5 R20 C4 r1-c2 r3-c3 putative RING zinc finger protein; 27623-28978 TC81762 AW622667 cLEX15P2 XIIID3 T4G5 R20 C7 r2-c2 r1-c4 {Arabidopsis thaliana}PIR|H96703|H96703 probable RIN Strong similarity to MRP-like ABC transporter TC81773 BE450653 cLEY14D7 XIIIG4 T4M7 R18 C13 r2-c2 r1-c4 gb|U92650 from A. thaliana and canalicular multi-drug alanine aminotransferase {Arabidopsis thaliana} TC81776 AW033989 cLEC29A19 IG8 T1M15 R12 C13 r1-c2 r3-c3 starch synthase, isoform V {Vigna unguiculata} TC81835 AI489258 cLED17F23 IIIB1 T1D1 R24 C4 r1-c2 r3-c3 ribulosebisphosphate carboxylase large subunit TC81850 AI897282 cLED26L23 IIID11 T1H21 R4 C8 r1-c2 r3-c3 acetyl-coA dehydrogenase, putative {Arabidopsis TC81857 AW737344 cTOD3O23 XIVB11 T4C22 R3 C3 r2-c2 r1-c4 thaliana} MADS box transcription factor MADS1 {Capsicum TC81862 BE353915 cTOD6P15 XXIC6 T6E11 R14 C5 r3-c1 r2-c4 annuum} tyrosine aminotransferase-like protein {Arabidopsis TC81863 AW928492 cTOC1J9 XVIID2 T5G3 R22 C7 r3-c2 r4-c4 thaliana} putative RING-H2 zinc finger protein ATL6 TC81880 AW622674 cLEX15P18 XIIID2 T4G3 R22 C7 r2-c2 r1-c4 {Arabidopsis thaliana} dihydrodipicolinate synthase {Nicotiana TC81883 BG127974 cTOF18L13 XIXC2 T5F3 R22 C6 r3-c2 r4-c4 tabacum}SP|Q42948|DAPA_TOBAC DIHYDRODIPICOLINATE SYNTHASE P putative CTP synthase {Oryza sativa} TC81887 BE450785 cLEY15I1 XIIIH6 T4O11 R14 C15 r2-c2 r1-c4 transcription factor-like; similar to CH6 and COP9 TC81893 AW034210 cLEC33E16 IIA1 T1A2 R23 C1 r1-c2 r3-c3 complex subunit 6 {Arabidopsis thaliana} putative phosphoribosylanthranilate transferase TC81895 AW029720 cLEC28K17 IG6 T1M11 R14 C13 r1-c2 r3-c3 {Arabidopsis thaliana}GP|7267861|emb|CAB78204.1||AL starch phosphorylase (AA 1-966) {Solanum tuberosum} TC81900 AI486229 cLED5N5 IVE1 T1J2 R23 C10 r1-c2 r3-c3 contains similarity to cyclopropane fatty acid TC81904 AW618853 cLPT17E8 XVH3 T4P5 R20 C16 r2-c2 r1-c4 synthase~gene_id: MEE5.5 {Arabidopsis thaliana} PROBABLE VACUOLAR ATP SYNTHASE TC81929 AW621415 cLEX11L22 XIIIB6 T4C11 R14 C3 r2-c2 r1-c4 SUBUNIT F (EC 3.6.1.34) (V-ATPASE F SUBUNIT) (VACUOLAR PROTON PUMP F cytochrome P450-like protein {Arabidopsis TC81940 AW617528 cLHT23L11 XXIB11 T6C21 R4 C3 r3-c1 r2-c4 thaliana}GP|7270932|emb|CAB80611.1||AL161595 cytochrome P cytochrome P450-like protein {Arabidopsis TC81993 AW617528 cLPT11J23 XVB9 T4D17 R8 C4 r2-c2 r1-c4 thaliana}PIR|T46196|T46196 cytochrome P450-like protein- uroporphyrinogen decarboxylase {Arabidopsis thaliana} TC81996 BG124909 cTOF7E17 XXF7 T5L14 R11 C12 r3-c2 r4-c4 succinate dehydrogenase flavoprotein alpha subunit TC82029 AW218470 cLEZ9G24 XIVG11 T4M22 R3 C13 r2-c2 r1-c4 {Arabidopsis thaliana}GP|8843734|dbj|BAA97282.1| HD-Zip protein {Arabidopsis TC82042 AW647780 cLEI2C10 VIID5 T2H9 R16 C8 r4-c2 r1-c3 thaliana}GP|3132474|gb|AAC16263.1||AC003096 homeodomain transcription f phosphate transporter{circumflex over ( )}{circumflex over ( )}putative phosphate TC82044 AI776381 cLER18E22 IXH5 T3O9 R16 C15 r2-c1 r4-c3 transporter{circumflex over ( )}{circumflex over ( )}inorganic phosphate transporter heat stress transcription factor A3 {Lycopersicon TC82048 AW399021 cLPT5B12 XVIB1 T4D2 R23 C4 r2-c2 r1-c4 peruvianum} putative glucosyl transferase {Arabidopsis TC82051 AI772146 cLER1F22 XA5 T3A10 R15 C1 r2-c1 r4-c3 thaliana}PIR|H84784|H84784 probable glucosyl transferase contains similarity to chalcone-flavonone isomerase TC82093 BG628492 cLEL22G17 XXIE9 T6I17 R8 C9 r3-c1 r2-c4 (chalcone isomerase)~gene_id: K18I23.7 {Arabidops phosphoribosylanthranilate isomerase {Arabidopsis TC82095 AW037478 cLET1I13 XIE8 T3J15 R12 C10 r2-c1 r4-c3 thaliana} LIN6{circumflex over ( )}acid invertase TC82103 AI779579 cLES8B13 XIA11 T3B21 R4 C2 r2-c1 r4-c3 Contains similarity to ARI, RING finger protein TC82118 AI484345 cLES1O17 XG5 T3M10 R15 C13 r2-c1 r4-c3 gb|X98309 from Drosophila melanogaster. ESTs gb|T44 transcription factor-like protein {Arabidopsis TC82130 BG643340 cTOF27E22 XXA1 T5B2 R23 C2 r3-c2 r4-c4 thaliana}GP|7576196|emb|CAB87947.1||AL163912 transcr polyphenol oxidase precursor TC82138 AW624791 cLEZ8M21 XIVG1 T4M2 R23 C13 r2-c2 r1-c4 bHLH transcription factor GBOF-1 {Tulipa gesneriana} TC82153 AI490119 cLED22C14 IIIC6 T1F11 R14 C6 r1-c2 r3-c3 glycerol-3-phosphate dehydrogenase {Arabidopsis TC82167 AI773999 cLER9I5 XC11 T3E22 R3 C5 r2-c1 r4-c3 thaliana}PIR|F84832|F84832 glycerol-3-phosphate deh putative cytochrome P450 {Oryza TC82169 AW624950 cLEZ9A23 XIVG9 T4M18 R7 C13 r2-c2 r1-c4 sativa}GP|11761117|dbj|BAB19107.1||AP002839 putative cytochrome P45 transcription factor IIA small subunit {Arabidopsis TC82195 BG126942 cTOF13L22 XVIIIH11 T5O22 R3 C15 r3-c2 r4-c4 thaliana}GP|5051786|emb|CAB45079.1||AL078637 tr glucosyltransferase-like protein {Arabidopsis TC82199 BF051083 cLEM21D15 VIIIA3 T2B6 R19 C2 r4-c2 r1-c3 thaliana}GP|7340661|emb|CAB82941.1||AL162506 putative chalcone synthase-like protein {Arabidopsis TC82205 AW623633 cTOB11H1 XVIG3 T4N6 R19 C14 r2-c2 r1-c4 thaliana}GP|7270436|emb|CAB80202.1||AL161586 chalcone s sugar transporter-like protein {Arabidopsis thaliana} TC82207 AW041746 cLET14I14 XID2 T3H3 R22 C8 r2-c1 r4-c3 putative cytochrome P450 {Arabidopsis TC82226 AW651015 cLEI15O17 VIIC9 T2F17 R8 C6 r4-c2 r1-c3 thaliana}GP|13877669|gb|AAK43912.1|AF370593_1|AF370593 putati putative zinc finger protein {Arabidopsis TC82243 AI781951 cLES17L23 XF4 T3K8 R17 C11 r2-c1 r4-c3 thaliana}GP|7270045|emb|CAB79860.1||AL161579 putative zin 2-oxoglutarate/malate translocator precursor {Spinacia TC82252 AW442880 cLET42G24 XXIA1 T6A1 R24 C1 r3-c1 r2-c4 oleracea}SP|Q41364|SOT1_SPIOL 2- OXOGLUTARATE NADH-dependent glutamate synthase {Arabidopsis TC82279 AW035530 cLEC39M7 XXIE2 T6I3 R22 C9 r3-c1 r2-c4 thaliana} anthocyanidin 3-O-glucosyltransferase {Petunia x TC82331 BG630259 cLEL33O12 XXIF10 T6K19 R6 C11 r3-c1 r2-c4 hybrida} 3-methylcrotonyl-CoA carboxylase non-biotinylated TC82338 BF098233 cLEW26M6 XIIG12 T3N24 R1 C14 r2-c1 r4-c3 subunit {Arabidopsis thaliana}GP|7021224|gb|AAF35 Cytochrome P450-like protein {Arabidopsis TC82348 AW738451 cTOD7I20 XVIIIA6 T5A12 R13 C1 r3-c2 r4-c4 thaliana}GP|7270098|emb|CAB79912.1||AL161580 Cytochrome P transketolase 1 {Capsicum TC82386 BF097344 cLEW20C18 XIIG1 T3N2 R23 C14 r2-c1 r4-c3 annuum}PIR|T09541|T09541 transketolase (EC 2.2.1.1) TKT1 precursor, chlor HEAT SHOCK FACTOR PROTEIN 5 (HSF 5) (HEAT TC82389 AW649996 cLEI11K12 IVH1 T1P2 R23 C16 r1-c2 r3-c3 SHOCK TRANSCRIPTION FACTOR 5) (HSTF 5).GP|6624614|emb|CAB Similar to Populus balsamifera subsp. trichocarpa X TC82393 BG627286 cLEL16O9 XXIC5 T6E9 R16 C5 r3-c1 r2-c4 Populus deltoides vegetative storage protein. (L putative enolase (2-phospho-D-glycerate hydroylase) TC82394 AW441644 cLEN17N4 IXB3 T3C5 R20 C3 r2-c1 r4-c3 {Arabidopsis thaliana}PIR|G84697|G84697 hypothe putative CCCH-type zinc finger protein {Arabidopsis TC82395 AI773737 cLER8C11 XG6 T3E12 R13 C5 r2-c1 r4-c3 thaliana}PIR|D84581|D84581 probable CCCH-type z 3-dehydroquinate synthase-like protein {Arabidopsis TC82414 AI774955 cLER13L4 IXE12 T3I23 R2 C9 r2-c1 r4-c3 thaliana} cytochrome P450-like protein {Arabidopsis TC82416 AW651396 cLEI16D15 XVIIE8 T5I15 R12 C9 r3-c2 r4-c4 thaliana}GP|7270932|emb|CAB80611.1||AL161595 cytochrome P isoflavone reductase homolog {Solanum TC82426 BG130065 cTOF29O11 XXB2 T5D6 R19 C4 r3-c2 r4-c4 tuberosum}SP|P52578|IFRH_SOLTU ISOFLAVONE REDUCTASE HOMOLOG ( putative pyrophosphate--fructose-6-phosphate 1- TC82429 BF051504 cLEM23M13 VIIIB11 T2D22 R3 C4 r4-c2 r1-c3 phosphotransferase {Arabidopsis thaliana}PIR|B84613| phosphoglycerate mutase {Solanum tuberosum} TC82433 BG643106 cTOF26J11 XIXH8 T5P15 R12 C16 r3-c2 r4-c4 6-phosphogluconate dehydrogenase, putative; 13029-14489 TC82459 BE450814 cLEY15O9 XIIIH10 T4O19 R6 C15 r2-c2 r1-c4 {Arabidopsis thaliana} putative P-protein: chorismate mutase, prephenate TC82472 BF050999 cLEM21C18 VIIIA2 T2B4 R21 C2 r4-c2 r1-c3 dehydratase {Arabidopsis thaliana} putative arginine methyltransferase {Arabidopsis TC82475 BF051059 cLEM21O8 VIIIA8 T2B16 R9 C2 r4-c2 r1-c3 thaliana} P450 hydroxylase {Petunia x TC82490 AI489137 cLED15E15 IIIA1 T1B1 R24 C2 r1-c2 r3-c3 hybrida}PIR|S32110|S32110 cytochrome P450 PET-1- garden petunia (fragm pathogenesis-related homeodomain protein (prhp) TC82493 AW618573 cLPT13P12 XVG11 T4N21 R4 C14 r2-c2 r1-c4 {Petroselinum crispum}SP|P48786|PRH_PETCR PATHOGENE ferredoxin--nitrite reductase {Nicotiana TC82500 AI775854 cLER16D16 IXG4 T3M7 R18 C13 r2-c1 r4-c3 tabacum}GP|19893|emb|CAA46940.1||X66145 ferredoxin--nitrit contains similarity to heat shock transcription TC82508 AW979619 cLEW8I23 XVIIIA8 T5A16 R9 C1 r3-c2 r4-c4 factor~gene_id: MOB24.9 {Arabidopsis thaliana} starch synthase {Ipomoea batatas} TC82511 AI899166 cLED37O8 XVIIC4 T5E7 R18 C5 r3-c2 r4-c4 alpha-glucosidase {Solanum tuberosum subsp. TC82534 AW648278 cLEI4E5 VIIE6 T2J11 R14 C10 r4-c2 r1-c3 tuberosum} similar to class I knotted-like homeodomain protein TC82559 AI490554 cLED25E14 IIID4 T1H7 R18 C8 r1-c2 r3-c3 (LeT6 putative internal rotenone-insensitive NADH TC82565 BG629691 cLEL29K7 XXIH1 T6O1 R24 C15 r3-c1 r2-c4 dehydrogenase {Solanum tuberosum} putative C3HC4-type RING zinc finger protein TC82567 AI778661 cLES6C1 XVIA6 T4B12 R13 C2 r2-c2 r1-c4 {Arabidopsis thaliana}GP|11908040|gb|AAG41449.1|AF3268 acetyl-CoA C-acetyltransferase {Arabidopsis thaliana} TC82576 BE459497 cLEM7A3 VIIIE7 T2J14 R11 C10 r4-c2 r1-c3 amidophosphoribosyltransferase {Arabidopsis thaliana} TC82583 AW154805 cLEW1C23 XIIE11 T3J22 R3 C10 r2-c1 r4-c3 putative anthocyanin 5-aromatic acyltransferase TC82613 AW092901 cLET22L23 XIIB6 T3D12 R13 C4 r2-c1 r4-c3 {Arabidopsis thaliana}PIR|G84823|G84823 probable an cystathionine beta-lyase {Solanum tuberosum} TC82650 BE461649 cLEG39D17 VIE7 T2I14 R11 C9 r4-c2 r1-c3 glutamine synthetase I {Medicago truncatula} TC82659 AI896662 cLEC16M12 ID10 T1G19 R6 C7 r1-c2 r3-c3 putative cytochrome P450; 1456-3294 {Arabidopsis TC82728 AW622085 cLEX14O19 XIIIC9 T4E17 R8 C5 r2-c2 r1-c4 thaliana}GP|10092278|gb|AAG12691.1|AC025814_15| AC0 HOMEOBOX-LEUCINE ZIPPER PROTEIN HAT22 TC82731 AW038246 cLET1H12 XIE7 T3J13 R12 C10 r2-c1 r4-c3 (HD-ZIP PROTEIN 22).GP|549887|gb|AAA56902.1||U09336 homeobox transcription factor inhibitor I kappa B homolog TC82775 BG124935 cTOF7K1 XXF11 T5L22 R3 C12 r3-c2 r4-c4 {Arabidopsis thaliana}GP|1773295|gb|AAC49611.1||U7 putative glycerol-3-phosphate dehydrogenase TC82784 AW219947 cLEX6M3 XIIIF2 T4K3 R22 C11 r2-c2 r1-c4 {Arabidopsis thaliana} NADH dehydrogenase like protein {Arabidopsis TC82792 AW040558 cLET7I22 XIIC4 T3F8 R17 C6 r2-c1 r4-c3 thaliana}GP|7268946|emb|CAB81256.1||AL161555 NADH dehy zinc finger protein SHI-like {Arabidopsis TC82801 AW216650 cLEC23D4 IIF8 T1K16 R9 C11 r1-c2 r3-c3 thaliana}GP|4929803|gb|AAD34162.1|AF152555_1|AF152555 put inorganic phosphate transporter TC82826 AW621975 cLEX13J24 XIIIC4 T4E7 R18 C5 r2-c2 r1-c4 polyneuridine aldehyde esterase {Rauvolfia serpentina} TC82834 BE433359 cLEG13E6 VE4 T2I7 R18 C9 r4-c2 r1-c3 alpha-glucosidase {Solanum tuberosum subsp. TC82868 AI487222 cLED6K9 IVB10 T1D20 R5 C4 r1-c2 r3-c3 tuberosum} ABC transporter-like protein {Arabidopsis TC82872 AW623019 cTOB8A15 XVIIB8 T5C15 R12 C3 r3-c2 r4-c4 thaliana}GP|13899119|gb|AAK48981.1|AF370554_1|AF370554 AB heat shock factor protein hsf24 (heat shock transcription TC82923 BF097217 cLEW19F16 XIIE2 T3J4 R21 C10 r2-c1 r4-c3 factor 24) (hstf 24) (heat stress transcri sugar transporter like protein {Arabidopsis TC82942 BG138983 cLPP11N17 XVD4 T4H7 R18 C8 r2-c2 r1-c4 thaliana}GP|2464913|emb|CAB16808.1||Z99708 sugar transp cytochrome P450-like protein {Arabidopsis TC82954 BE450630 cLEY14M8 XIIIG8 T4M15 R12 C13 r2-c2 r1-c4 thaliana}PIR|T47554|T47554 cytochrome P450 homolog F8J2.1 TRYPTOPHAN SYNTHASE BETA CHAIN 2 TC82960 BE458808 cLEM4L3 VIIID9 T2H18 R7 C8 r4-c2 r1-c3 PRECURSOR (EC 4.2.1.20).GP|2792520|gb|AAB97087.1||AF042320 tryptop putative C3HC4-type RING zinc finger protein TC82965 AW621441 cLEX12A9 XIIIB9 T4C17 R8 C3 r2-c2 r1-c4 {Arabidopsis thaliana}PIR|B84813|B84813 probable RING Similar to gb|Z84571 anthranilate N- TC82992 BG133540 cTOE13N21 XIIF6 T3L12 R13 C12 r2-c1 r4-c3 hydroxycinnamoyl/benzoyltransferase from Dianthus caryophyllus. ABC transporter homolog {Populus nigra} TC83000 AW033000 cLEC19N6 XVIIC9 T5E17 R8 C5 r3-c2 r4-c4 contains similarity to ABC TC83006 BG141252 cLPP20D10 XVE6 T4J11 R14 C10 r2-c2 r1-c4 transporter~gene_id: MAC9.4 {Arabidopsis thaliana} putative strictosidine synthase TC83008 BG128579 cTOF21M10 XIXE5 T5J9 R16 C10 r3-c2 r4-c4 phosphate/phosphoenolpyruvate translocator precursor TC83014 BE460073 cLEM8L2 VIIIF6 T2L12 R13 C12 r4-c2 r1-c3 {Nicotiana tabacum}GP|1778145|gb|AAB40648.1||U putative enolase; 31277-33713 {Arabidopsis TC83066 AW648181 cLEI3N19 VIIE2 T2J3 R22 C10 r4-c2 r1-c3 thaliana}PIR|B96768|B96768 protein enolase F2P9.10 [impo diacylglycerol kinase {Lycopersicon esculentum} TC83073 AW223728 cLEN12N22 VIIIG11 T2N22 R3 C14 r4-c2 r1-c3 cytochrome P450 {Capsicum annuum} TC83085 AW219261 cLEX3H20 XIIID12 T4G23 R2 C7 r2-c2 r1-c4 contains similarity to RNA polymerase transcriptional TC83117 AW218226 cLEZ1O15 XIVF9 T4K18 R7 C11 r2-c2 r1-c4 regulation mediator~gene_id: MHC9.3 {Arabidopsi acetyl-CoA synthetase, putative; 45051-31547 TC83139 AW647759 cLEI2M11 VIID7 T2H13 R12 C8 r4-c2 r1-c3 {Arabidopsis thaliana}PIR|D96595|D96595 probable acety ABC transporter-like protein {Arabidopsis TC83143 AW038363 cLET6E16 XIIB12 T3D24 R1 C4 r2-c1 r4-c3 thaliana}PIR|T07717|T07717 probable ABC-type transport pr putative sugar transporter {Arabidopsis thaliana} TC83157 BG132543 cTOE7P6 XVIIIG2 T5M4 R21 C13 r3-c2 r4-c4 putative zinc finger protein {Arabidopsis TC83165 BE436795 cLEG34A24 VIB12 T2C24 R1 C3 r4-c2 r1-c3 thaliana}GP|7270045|emb|CAB79860.1||AL161579 putative zin CYTOCHROME P450 98A2 (EC 1.14.—.—). TC83207 BE436335 cLEG32E11 VIA12 T2A24 R1 C1 r4-c2 r1-c3 GP|2738998|gb|AAB94587.1||AF022458 CYP98A2p {Glycine max}PIR|T0 transcription factor, putative {Arabidopsis TC83217 BE458948 cLEM5G9 VIIID12 T2H24 R1 C8 r4-c2 r1-c3 thaliana}PIR|E96612|E96612 probable transcription facto auxin-induced basic helix-loop-helix transcription factor TC83218 BG130684 cTOF31L2 XXC6 T5F12 R13 C6 r3-c2 r4-c4 {Gossypium hirsutum} ABC transporter-like protein {Arabidopsis TC83254 BE434861 cLEG24A21 VG6 T2M11 R14 C13 r4-c2 r1-c3 thaliana}GP|9964121|gb|AAG09829.1|AF287699_1|AF287699 hal bHLH transcription factor JAF13 {Petunia x hybrida} TC83264 BE433296 cLEG13C11 XVIIF11 T5K21 R4 C11 r3-c2 r4-c4 glycerol-3-phosphate dehydrogenase {Arabidopsis TC83308 BE431781 cLEG3E11 VIE11 T2I22 R3 C9 r4-c2 r1-c3 thaliana}PIR|F84832|F84832 glycerol-3-phosphate deh cytochrome p450 lxxia3 {Solanum TC83334 BG631413 cLEL7M4 XXH7 T5P14 R11 C16 r3-c2 r4-c4 melongena}SP|P37119|C713_SOLME CYTOCHROME P450 71A3 (EC 1.14.—.—) ( putative 6-phosphogluconolactonase {Arabidopsis TC83350 AW622762 cTOB5D8 XVIIB4 T5C7 R18 C3 r3-c2 r4-c4 thaliana} soluble starch (bacterial glycogen) synthase {Solanum TC83359 BE432874 cLEG10I6 VD4 T2G7 R18 C7 r4-c2 r1-c3 tuberosum}SP|P93568|UGS2_SOLTU SOLUBLE GLYCOG beta-amylase-like {Arabidopsis thaliana} TC83371 BE433215 cLEG12B22 VD10 T2G19 R6 C7 r4-c2 r1-c3 cytochrome P450 {Arabidopsis TC83399 AI896822 cLEC23P7 IF3 T1K5 R20 C11 r1-c2 r3-c3 thaliana}GP|7268718|emb|CAB78925.1||AL161550 cytochrome P450 {Arabidop fructokinase {Lycopersicon TC83425 BG139714 cLPP14C5 XVD9 T4H17 R8 C8 r2-c2 r1-c4 esculentum}GP|2102691|gb|AAB57733.1||U64817 fructokinase {Lycopersicon e putative citrate synthase {Arabidopsis TC83487 BE434567 cLEG18A23 VF7 T2K13 R12 C11 r4-c2 r1-c3 thaliana}PIR|C84858|C84858 probable citrate synthase [import putative acetone-cyanohydrin lyase {Arabidopsis TC83491 AW219332 cLEX4G11 XIIIE5 T4I9 R16 C9 r2-c2 r1-c4 thaliana}PIR|T01151|T01151 probable acetone-cyanohy putative pyrophosphate-dependent phosphofructo-1- TC83500 AW738248 cTOD6B4 XVIIH12 T5O23 R2 C15 r3-c2 r4-c4 kinase {Arabidopsis thaliana} uroporphyrinogen decarboxylase {Arabidopsis thaliana} TC83506 BG129172 cTOF23D19 XIXF8 T5L15 R12 C12 r3-c2 r4-c4 Zn finger protein {Nicotiana TC83522 AI489847 cLED15J6 IIIA5 T1B9 R16 C2 r1-c2 r3-c3 tabacum}GP|1360078|emb|CAA66601.1||X97942 Zn finger protein {Nicotiana transcription factor WRKY6 {Arabidopsis TC83553 AW029692 cLEC11I13 IC3 T1E5 R20 C5 r1-c2 r3-c3 thaliana}GP|12658412|gb|AAK01128.1|AF331713_1|AF331713 tran limonene cyclase like protein {Arabidopsis TC83555 AW932587 cLEF49C20 VA1 T2A1 R24 C1 r4-c2 r1-c3 thaliana}GP|2245029|emb|CAB10449.1||Z97341 limonene cycl GMP synthase; 61700-64653 {Arabidopsis TC83694 AW616601 cLHT11H8 XIVH7 T4O14 R11 C15 r2-c2 r1-c4 thaliana}PIR|E96661|E96661 GMP synthase, 61700-64653 [import beta-amylase {Glycine TC83696 AW616937 cLHT18H3 XVA7 T4B13 R12 C2 r2-c2 r1-c4 max}GP|902938|dbj|BAA09462.1||D50866 beta- amylase {Glycine max} pyruvate kinase (EC 2.7.1.40) A, chloroplast-common TC83701 BE459930 cLEM8O6 VIIIF11 T2L22 R3 C12 r4-c2 r1-c3 tobacco cytochrome p450-like protein {Arabidopsis TC83712 AW616143 cLHT6I19 XVC12 T4F23 R2 C6 r2-c2 r1-c4 thaliana}GP|7270718|emb|CAB80401.1||AL161591 cytochrome p Putative UDP-glucose glucosyltransferase {Arabidopsis TC83719 AW616197 cLHT1O22 XVA11 T4B21 R4 C2 r2-c2 r1-c4 thaliana}PIR|H86356|H86356 probable UDP-gluco Similar to gb|Z84386 anthranilate N- TC83737 AW650590 cLEI13B9 VIIB6 T2D11 R14 C4 r4-c2 r1-c3 hydroxycinnamoyl/benzoyltransferase from Dianthus caryophyllus. Phosphoglycerate dehydrogenase-like protein TC83740 AW650696 cLEI13H4 VIIB11 T2D21 R4 C4 r4-c2 r1-c3 {Arabidopsis thaliana}GP|7270370|emb|CAB80137.1||AL1615 phosphoribosyl pyrophosphate synthase isozyme 4 TC83753 AW623660 cTOB11L23 XVIG6 T4N12 R13 C14 r2-c2 r1-c4 {Spinacia oleracea} putative dihydroflavonol reductase {Oryza sativa} TC83761 AW623558 cTOB11G1 XVIG2 T4N4 R21 C14 r2-c2 r1-c4 hexose transporter TC83763 AI776698 cLER19B17 IXH11 T3O21 R4 C15 r2-c1 r4-c3 tyrosine/dopa decarboxylase {Thalictrum flavum subsp. TC83804 AW617134 cLHT21B22 XVA12 T4B23 R2 C2 r2-c2 r1-c4 glaucum} Cytochrom P450-like protein {Arabidopsis TC83813 AW617348 cLHT22P7 XVB2 T4D3 R22 C4 r2-c2 r1-c4 thaliana}PIR|T46159|T46159 cytochrome P450-like protein- glycolate oxidase {Arabidopsis thaliana} TC83832 BE449563 cLHT31P20 XVC6 T4F11 R14 C6 r2-c2 r1-c4 alpha-glucan phosphorylase, h isozyme phosphorylase TC83865 AI775729 cLER16K20 IXG8 T3M15 R12 C13 r2-c1 r4-c3 h) {Solanum tuberosum}SP|P32811|PHSH_SOLTU ALPH CYTOCHROME P450 98A3 (EC 1.14.—.—). TC83866 AI775624 cLER16G13 IXG5 T3M9 R16 C13 r2-c1 r4-c3 GP|2623303|gb|AAB86449.1||AC002409 putative cytochrome P450 {Ara general negative transcription regulator-like TC83872 BG139930 cLPP15E1 XVD11 T4H21 R4 C8 r2-c2 r1-c4 {Arabidopsis thaliana} Dof zinc finger protein {Nicotiana TC83881 AI894749 cLEC5D8 IID11 T1G22 R3 C7 r1-c2 r3-c3 tabacum}PIR|T02203|T02203 finger protein Dof- common tobacco (f putative ABC transporter {Arabidopsis TC83901 AW930474 cLEF42N1 IVF11 T1L22 R3 C12 r1-c2 r3-c3 thaliana}GP|4115931|gb|AAD03441.1||AF118223 contains similari ornithine carbamoyltransferase; OCTase {Canavalia TC83905 BG127833 cTOF18A20 XIXB7 T5D13 R12 C4 r3-c2 r4-c4 lineata}GP|12003188|gb|AAG43481.1|AF203688_1|AF20 succinate dehydrogenase iron-protein subunit TC83937 BG131824 cTOE5K6 XVIIIF10 T5K20 R5 C11 r3-c2 r4-c4 {Arabidopsis thaliana} tyrosine aminotransferase {Arabidopsis thaliana} TC83980 AW737817 cTOD4I20 XVIIH3 T5O5 R20 C15 r3-c2 r4-c4 ferredoxin--nitrite reductase {Nicotiana TC83986 AI776320 cLER18K1 IXH9 T3O17 R8 C15 r2-c1 r4-c3 tabacum}GP|861067|emb|CAA46942.1||X66147 ferredoxin--nitri legumin-like protein {Arabidopsis TC84014 BE344407 cLEY7I19 XIVC10 T4E20 R5 C5 r2-c2 r1-c4 thaliana}PIR|H84687|H84687 legumin-like protein [imported]-Arab MADS transcriptional factor; STMADS16 {Solanum TC84038 AW929235 cTOC6J20 XVIIE7 T5I13 R12 C9 r3-c2 r4-c4 tuberosum}PIR|T06995|T06995 probable MADS box transc amidophosphoribosyltransferase {Arabidopsis thaliana} TC84044 AI775377 cLER15G24 IXF9 T3K17 R8 C11 r2-c1 r4-c3 transketolase 1 {Capsicum TC84048 BF051161 cLEM21D4 VIIIA4 T2B8 R17 C2 r4-c2 r1-c3 annuum}PIR|T09541|T09541 transketolase (EC 2.2.1.1) TKT1 precursor, chlor UDP-GLUCOSE 4-EPIMERASE GEPI48 (EC 5.1.3.2) TC84055 AW221109 cLEF12H9 IVD12 T1H24 R1 C8 r1-c2 r3-c3 (GALACTOWALDENASE) (UDP-GALACTOSE 4- EPIMERASE).GP|3021 contains similarity to chorismate mutase-T and TC84057 BF051293 cLEM22K9 VIIIB4 T2D8 R17 C4 r4-c2 r1-c3 prephenate dehydrogenase~gene_id: MGG23.1 {Arabidopsis Strong similarity to gb|Z50851 HD-zip (athb-8) gene TC84068 BF050867 cLEM19F10 VIIH6 T2P11 R14 C16 r4-c2 r1-c3 from Arabidopsis thaliana containing Homeobox PF Is a member of the PF|00044 glyceraldehyde 3- TC84078 AW034065 cLEC37K13 IIC4 T1E8 R17 C5 r1-c2 r3-c3 phosphate dehydrogenase family. ESTs gb|T43985, gb|N38 putative hydroxymethylglutaryl-CoA lyase TC84085 AW031371 cLEC40O17 IID8 T1G16 R9 C7 r1-c2 r3-c3 {Arabidopsis thaliana}PIR|T02655|T02655 hydroxymethylgluta putative anthranilate N- TC84103 AW217704 cTOC6A19 XVIIE3 T5I5 R20 C9 r3-c2 r4-c4 hydroxycinnamoyl/benzoyltransferase {Arabidopsis thaliana}PIR|T00527|T00527 RING zinc finger protein-like {Arabidopsis thaliana} TC84140 AW649904 cLEI11E13 VIIA10 T2B19 R6 C2 r4-c2 r1-c3 CCAAT box binding factor/transcription factor Hap2a TC84198 BF113081 cLEG43E15 VIF12 T2K24 R1 C11 r4-c2 r1-c3 {Arabidopsis thaliana}PIR|T49898|T49898 CCAAT MADS-box transcription factor FBP24 {Petunia x TC84232 AI486443 cLED8C18 IVC6 T1F12 R13 C6 r1-c2 r3-c3 hybrida} adenylosuccinate lyase-like protein; 104558-106845 TC84319 BG134019 cTOE15E21 XVIIIC10 T5E20 R5 C5 r3-c2 r4-c4 {Arabidopsis thaliana}PIR|B86484|B86484 hypothet pyruvate kinase-like protein {Arabidopsis TC84320 BG133998 cTOE15C1 XVIIIC8 T5E16 R9 C5 r3-c2 r4-c4 thaliana}PIR|T47556|T47556 pyruvate kinase-like protein- unnamed protein product TC84322 BG133901 cTOE14B12 XVIIIC3 T5E6 R19 C5 r3-c2 r4-c4 {unidentified}GP|2462911|emb|CAB06081.1||Z83832 UDP-glucose:sterol glucosyl folypolyglutamate synthase-like protein {Arabidopsis TC84330 BG133283 cTOE11N8 XVIIIB11 T5C22 R3 C3 r3-c2 r4-c4 thaliana} dihydroxy-acid dehydratase {Arabidopsis thaliana} TC84340 BG134687 cTOE17J11 XVIIID4 T5G8 R17 C7 r3-c2 r4-c4 CTP synthase like protein {Arabidopsis TC84368 AW980043 cLEW8A6 XIIH11 T3P22 R3 C16 r2-c1 r4-c3 thaliana}GP|7268827|emb|CAB79032.1||AL161552 CTP synthase li Putative acyl-CoA:1-acylglycerol-3-phosphate TC84467 BG135571 cTOE23A11 XVIIIE7 T5I14 R11 C9 r3-c2 r4-c4 acyltransferase {Arabidopsis thaliana}PIR|D96550|D965 putative gluconokinase {Arabidopsis TC84507 AI773430 cLER7C7 XC5 T3E10 R15 C5 r2-c1 r4-c3 thaliana}PIR|C84544|C84544 probable gluconokinase [imported]- Strong similarity to F19I3.2 GP|3033375 putative TC84522 AI772745 cLER3P15 XB9 T3C18 R7 C3 r2-c1 r4-c3 berberine bridge enzyme from Arabidopsis thaliana B homeodomain-leucine zipper protein 57 {Glycine max} TC84550 AW398295 cLPT2L23 XVIA4 T4B8 R17 C2 r2-c2 r1-c4 transcription factor {Nicotiana tabacum} TC84557 BG642494 cTOD11G2 XVIIG1 T5M1 R24 C13 r3-c2 r4-c4 carbamoyl-phosphate synthetase small subunit TC84578 AW738069 cTOD5K3 XVIIH10 T5O19 R6 C15 r3-c2 r4-c4 {Arabidopsis thaliana} hexose transporter{circumflex over ( )}{circumflex over ( )}hexose transporter TC71791 BG134154 cTOE15O14 XVIIIC11 T5E22 R3 C5 r3-c2 r4-c4 protein{circumflex over ( )}{circumflex over ( )}pathogenesis-related protein P4{circumflex over ( )}{circumflex over ( )}pathogenesis-related protein PR1a (P4) 33 kDa precursor protein of oxygen-evolving complex TC71796 BG128633 cTOF21H21 XIXE3 T5J5 R20 C10 r3-c2 r4-c4 ADP-glucose pyrophosphorylase small subunit TC71797 AI781653 cLES16N17 XF2 T3K4 R21 C11 r2-c1 r4-c3 glutamine synthetase TC71798 AI490202 cLER1O9 XA12 T3A24 R1 C1 r2-c1 r4-c3 cytochrome P450 like_TBP {Nicotiana TC71805 BG138584 cLPP10E22 XVD2 T4H3 R22 C8 r2-c2 r1-c4 tabacum}GP|1545805|dbj|BAA10929.1||D64052 cytochrome P450 like fructose-bisphosphate aldolase {Persea americana} TC71818 AI774641 cLER12N18 IXE9 T3I17 R8 C9 r2-c1 r4-c3 plastidic aldolase NPALDP1 {Nicotiana paniculata} TC71821 BE433579 cLEG16G20 VE11 T2I21 R4 C9 r4-c2 r1-c3 glutamate decarboxylase {Petunia TC71841 AI776639 cLER19E4 XA1 T3A2 R23 C1 r2-c1 r4-c3 hybrida}SP|Q07346|DCE_PETHY GLUTAMATE DECARBOXYLASE (EC 4.1.1.15) phenylalanine ammonia lyase TC71847 AW034774 cLEC32C18 IH7 T1O13 R12 C15 r1-c2 r3-c3 glutamate decarboxylase isozyme 1 {Nicotiana TC71868 BG138366 cLPP9O23 XVF8 T4L15 R12 C12 r2-c2 r1-c4 tabacum} plastidic aldolase {Nicotiana paniculata} TC71875 AI782836 cLES20N20 XG10 T3M20 R5 C13 r2-c1 r4-c3 fructose-bisphosphate aldolase {Persea americana} TC71877 AW650010 cLEI11M24 VA7 T2A13 R12 C1 r4-c2 r1-c3 ADENINE PHOSPHORIBOSYLTRANSFERASE 1 TC71878 BG123164 cTOF1E19 XIXD1 T5H1 R24 C8 r3-c2 r4-c4 (EC 2.4.2.7) (APRT).GP|16164|emb|CAA41497.1||X58640 adenine ph ribulose 1,5-bisphosphate carboxylase/oxygenase small TC71908 AW217485 cTOB1E19 XVIIA9 T5A17 R8 C1 r3-c2 r4-c4 subunit{circumflex over ( )}{circumflex over ( )}ribulose 1,5-bisphosphate carboxylase/oxyenase ribulose-1,5-bisphosphate carboxylase, small subunit TC71912 AI782070 cLES18C15 XF7 T3K14 R11 C11 r2-c1 r4-c3 precursor{circumflex over ( )}{circumflex over ( )}ribulose 1,5-bisphosphate carboxylase/oxygenase{circumflex over ( )}{circumflex over ( )}ribulose-1,5-bisphophate carboxylase/oxygenase small subunit phosphoribosyl diphosphate synthase {Arabidopsis TC71917 AW442702 cLEM8K21 XIIA1 T3B2 R23 C2 r2-c1 r4-c3 thaliana}GP|4512664|gb|AAD21718.1||AC006931 putati glutamate dehydrogenase TC71919 AI896071 cLEC13D4 IC9 T1E17 R8 C5 r1-c2 r3-c3 ribulose bisphosphate carboxylase small subunit 1 TC71926 AI774466 cLER12M6 IXE8 T3I15 R12 C9 r2-c1 r4-c3 precursor {Lycopersicon esculentum}SP|P08706|RBS1 plastidic aldolase NPALDP1 {Nicotiana paniculata} TC71931 BE432437 cLEG8C18 VIH10 T2O20 R5 C15 r4-c2 r1-c3 spermine synthase 1 {Datura TC71984 AW622878 cTOB5N16 XVIIB6 T5C11 R14 C3 r3-c2 r4-c4 stramonium}SP|Q96556|SPE1_DATST SPERMIDINE SYNTHASE 1 (EC 2.5.1.16) (PU glutamine synthetase {Lycopersicon esculentum} TC71994 BF098111 cLEW25D9 XIIG8 T3N16 R9 C14 r2-c1 r4-c3 glutamate decarboxylase isozyme 1 {Nicotiana TC71998 AW625743 cLEZ16B12 XIVD9 T4G18 R7 C7 r2-c2 r1-c4 tabacum} beta-fructosidase TC72004 AI894871 cLEC6K3 IIE9 T1I18 R7 C9 r1-c2 r3-c3 acid invertase, AI {EC 3.2.1.26} [Lycopersicon TC72005 BF051964 cLEM24F2 VIIIC4 T2F8 R17 C6 r4-c2 r1-c3 esculentum = tomatoes, cv. Super First, fruits, Peptide, 636 aa]{circumflex over ( )}{circumflex over ( )}vacuolar invertase precursor{circumflex over ( )}{circumflex over ( )}beta- fructofuranosidase beta-fructofuranosidase precursor {Lycopersicon TC72006 BE431858 cLEG4M7 VIH2 T2O4 R21 C15 r4-c2 r1-c3 esculentum}SP|P29000|INVA_LYCES ACID BETA- FRUCTOFUR beta-fructofuranosidase precursor {Lycopersicon TC72007 BE432922 cLEG10J17 VD5 T2G9 R16 C7 r4-c2 r1-c3 esculentum}SP|P29000|INVA_LYCES ACID BETA- FRUCTOFUR enolase TC72015 BE460442 cLEG29K14 VH11 T2O21 R4 C15 r4-c2 r1-c3 threonine deaminase TC72016 BE459391 cLEM6N9 VIIIE6 T2J12 R13 C10 r4-c2 r1-c3 ubiquinol--cytochrome-c reductase (EC 1.10.2.2) Rieske TC72021 AW033888 cLEC32O14 IVG8 T1N16 R9 C14 r1-c2 r3-c3 iron-sulfur protein - potato polyphenol oxidase precursor TC72054 AW033927 cLEC37G14 IIC1 T1E2 R23 C5 r1-c2 r3-c3 polyphenol oxidase precursor TC72055 AW626331 cLEZ19D8 XIVF4 T4K8 R17 C11 r2-c2 r1-c4 polyphenol oxidase precursor TC72056 AI897921 cLED31I5 XVID1 T4H2 R23 C8 r2-c2 r1-c4 polyphenoloxidase, P2 [Lycopersicon TC72057 AI773100 cLER5I14 XVIB7 T4D14 R11 C4 r2-c2 r1-c4 esculentum = tomatoes, cv Tiny Tim LA154, flowers, Peptide Chloroplast, 587 aa]{circumflex over ( )}{circumflex over ( )}polyphenol oxidase precursor vacuolar ATP synthase subunit b isoform 1 subunit) TC72080 AI487183 cLED9M8 IVD1 T1H2 R23 C8 r1-c2 r3-c3 {Gossypium hirsutum}SP|Q43432|VAT1_GOSHI VACUOLA cytochrome p450 lxxvia2 {Solanum TC72085 AI895030 cLEC6H17 IIE8 T1I16 R9 C9 r1-c2 r3-c3 melongena}SP|P37122|C762_SOLME CYTOCHROME P450 76A2 (EC 1.14.—.—) ethylene-responsive methionine synthase TC72099 AW429057 cTOA1I20 XVIE9 T4J18 R7 C10 r2-c2 r1-c4 cinnamic acid 4-hydroxylase {Capsicum annuum} TC72100 BE435434 cLEG26P11 VG11 T2M21 R4 C13 r4-c2 r1-c3 cinnamic acid 4-hydroxylase {Capsicum chinense} TC72101 BE435368 cLEG26M11 IB4 T1C7 R18 C3 r1-c2 r3-c3 glyceraldehyde 3-phosphate dehydrogenase b precursor, TC72118 AW039016 cLET12C15 XIC7 T3F13 R12 C6 r2-c1 r4-c3 chloroplast {Pisum sativum}SP|P12859|G3PB_PEA glyceraldehyde 3-phosphate dehydrogenase b precursor, TC72119 AI775099 cLER14D17 IXF3 T3K5 R20 C11 r2-c1 r4-c3 chloroplast {Pisum sativum}SP|P12859|G3PB_PEA 4-hydroxyphenylpyruvate dioxygenase {Solenostemon TC72120 BE460965 cLEG37G9 VID10 T2G20 R5 C7 r4-c2 r1-c3 scutellarioides} 4-hydroxyphenylpyruvate dioxygenase {Solenostemon TC72121 AW035977 cLEC33J10 IIA3 T1A6 R19 C1 r1-c2 r3-c3 scutellarioides} obtusifoliol 14-alpha-demethylase {Triticum TC72126 AI773859 cLER8M8 XVIIA12 T5A23 R2 C1 r3-c2 r4-c4 aestivum}SP|P93596|CP51_WHEAT CYTOCHROME P450 51 (EC 1. fructokinase 1 {Arabidopsis TC72131 BG139399 cLPP13C23 XVD6 T4H11 R14 C8 r2-c2 r1-c4 thaliana}GP|13878053|gb|AAK44104.1|AF370289_1|AF370289 putative fructok beta-glucosidase {Arabidopsis thaliana} TC72139 AW651266 cLEI16I11 VIID1 T2H1 R24 C8 r4-c2 r1-c3 AP2 domain containing protein {Prunus armeniaca} TC72156 AW441232 cLEN13E14 VIIIH4 T2P8 R17 C16 r4-c2 r1-c3 leucine zipper-containing protein AT103 {Arabidopsis TC72159 BG124441 cTOF5C10 XXE10 T5J20 R5 C10 r3-c2 r4-c4 thaliana}PIR|T47754|T47754 leucine zipper-cont proline oxidase precursor {Arabidopsis thaliana} TC72165 cLED18A19 cLED18A19 IVB4 T1D8 R17 C4 r1-c2 r3-c3 homeobox TC72179 AW441945 cLEN19I1 IXB9 T3C17 R8 C3 r2-c1 r4-c3 cytosolic aconitase {Nicotiana tabacum} TC72186 AI775579 cLER15P4 IXG1 T3M1 R24 C13 r2-c1 r4-c3 cytosolic aconitase {Nicotiana tabacum} TC72187 AW040810 cLET10D11 XIC1 T3F1 R24 C6 r2-c1 r4-c3 hypothetical Cys-3-His zinc finger protein {Arabidopsis TC72194 BE434577 cLEG18C23 VF8 T2K15 R12 C11 r4-c2 r1-c3 thaliana}GP|6598933|gb|AAF18728.1|AC018721_(—) aminotransferase-like protein {Arabidopsis thaliana} TC72199 AW033908 cLEC27G7 IG1 T1M1 R24 C13 r1-c2 r3-c3 PROBABLE VACUOLAR ATP SYNTHASE TC72206 BE436940 cLEG34P7 VIC5 T2E10 R15 C5 r4-c2 r1-c3 SUBUNIT D 2 (EC 3.6.1.34) (V-ATPASE D SUBUNIT 2) (VACUOLAR PROTON PUM malate dehydrogenase, glyoxysomal precursor TC72213 BG123651 cTOF2L11 XXB8 T5D16 R9 C4 r3-c2 r4-c4 {Citrullus vulgaris}EGAD|130842|139627 glyoxysomal mala w-3 desaturase {Solanum TC72222 BE436518 cLEG33A5 VIB5 T2C10 R15 C3 r4-c2 r1-c3 tuberosum}PIR|T07685|T07685 omega-3 fatty acid desaturase (EC 1.14.99.—)- ATP synthase gamma subunit, mitochondrial precursor TC72225 BE459571 cLEM7M13 VIIIE12 T2J24 R1 C10 r4-c2 r1-c3 {Ipomoea batatas}SP|P26360|ATP3_IPOBA ATP SYNTH nucleoside diphosphate kinase TC72228 AW621401 cLEX11J10 XIIIB3 T4C5 R20 C3 r2-c2 r1-c4 glutamine synthetase TC72235 BG124516 cTOF5D22 XXE11 T5J22 R3 C10 r3-c2 r4-c4 sulfite reductase {Nicotiana TC72279 BE458560 cLEM2D21 VIIID1 T2H2 R23 C8 r4-c2 r1-c3 tabacum}GP|3721540|dbj|BAA33531.1||D83583 Sulfite Reductase {Nicotiana ALTERNATIVE OXIDASE 1 PRECURSOR (EC 1.—.—. TC72280 BG136312 cLPP2C18 XVE7 T4J13 R12 C10 r2-c2 r1-c4 —).GP|558054|gb|AAC60576.1||S71335 alternative oxidase, A homologous to glucosyltransferases TC72286 AI898951 cLED36O17 IIIH3 T1P5 R20 C16 r1-c2 r3-c3 CYTOCHROME P450 81E1 (EC 1.14.—.—) TC72288 AW034115 cLEC33I16 XVA10 T4B19 R6 C2 r2-c2 r1-c4 (ISOFLAVONE 2′-HYDROXYLASE) (P450 91A4) (CYP GE-3).GP|2443348|db UDP-GLUCOSE 4-EPIMERASE (EC 5.1.3.2) TC72291 AW219913 cLEX6I21 XIIIF1 T4K1 R24 C11 r2-c2 r1-c4 (GALACTOWALDENASE) (UDP-GALACTOSE 4- EPIMERASE).GP|8698725|gb| transaldolase TC72292 AW621229 cLEX11O7 XIIIB7 T4C13 R12 C3 r2-c2 r1-c4 transcription factor {Vicia TC72300 BE435913 cLEG30M14 VIA4 T2A8 R17 C1 r4-c2 r1-c3 faba}GP|2104681|emb|CAA66481.1||X97907 transcription factor {Vicia faba putative CONSTANS-like B-box zinc finger protein TC72313 BG129862 cTOF28H9 XXA10 T5B20 R5 C2 r3-c2 r4-c4 {Arabidopsis thaliana}PIR|A84720|A84720 hypothetic glucose-6-phosphate 1-dehydrogenase {Solanum TC72317 AW929634 cTOC9N19 XIIIA4 T4A7 R18 C1 r2-c2 r1-c4 tuberosum}SP|P37830|G6PD_SOLTU GLUCOSE-6- PHOSPHATE 1-D glucose-6-phosphate 1-dehydrogenase {Solanum TC72318 AI894720 cLEC5K16 IIE1 T1I2 R23 C9 r1-c2 r3-c3 tuberosum}SP|P37830|G6PD_SOLTU GLUCOSE-6- PHOSPHATE 1-D pyruvate kinase-like protein {Arabidopsis TC72325 BG135918 cLPP1E21 XVE4 T4J7 R18 C10 r2-c2 r1-c4 thaliana}PIR|T47556|T47556 pyruvate kinase-like protein- beta-amylase {Prunus armeniaca} TC72330 BG136584 cLPP2H4 VB8 T2C15 R12 C3 r4-c2 r1-c3 glucose-6-phosphate isomerase, cytosolic 1 (gpi) TC72335 BG129054 cTOF23M19 XIXG2 T5N3 R22 C14 r3-c2 r4-c4 (phosphoglucose isomerase) (pgi) (phosphohexose iso AP2 domain-containing transcription factor {Nicotiana TC72337 AW221854 cLEN4I21 IXC11 T3E21 R4 C5 r2-c1 r4-c3 tabacum} pyruvate dehydrogenase E1 beta subunit isoform 1 {Zea TC72349 BE431827 cLEG4E1 VIG12 T2M24 R1 C13 r4-c2 r1-c3 mays} fructose-1,6-bisphosphatase, cytosolic bisphosphate 1- TC72350 BG127847 cTOF18E4 XIXB10 T5D19 R6 C4 r3-c2 r4-c4 phosphohydrolase) (fbpase) (cy-fl) {Solanum tu fructose-1,6-bisphosphatase, cytosolic bisphosphate 1- TC72351 BG123415 cTOF1J18 XIXD5 T5H9 R16 C8 r3-c2 r4-c4 phosphohydrolase) (fbpase) (cy-fl) {Solanum tu isopentenyl diphosphate isomerase 1 {Nicotiana TC72352 AW616688 cLHT12K1 XVA1 T4B1 R24 C2 r2-c2 r1-c4 tabacum} putative glucose regulated repressor protein TC72370 AW455273 cLEX10M20 XIIIA9 T4A17 R8 C1 r2-c2 r1-c4 {Arabidopsis thaliana}PIR|A84649|A84649 probable gluco pyruvate dehydrogenase E1 alpha subunit {Arabidopsis TC72372 AW039459 cLET10E22 XIC2 T3F3 R22 C6 r2-c1 r4-c3 thaliana} PYROPHOSPHATE-FRUCTOSE 6-PHOSPHATE 1- TC72375 BF051072 cLEM21B13 VIIH12 T2P23 R2 C16 r4-c2 r1-c3 PHOSPHOTRANSFERASE BETA SUBUNIT (EC 2.7.1.90) (PFP) (6-PHOSPHO transketolase, chloroplast precursor {Solanum TC72376 BG128738 cTOF21N8 VIIG5 T2N9 R16 C14 r4-c2 r1-c3 tuberosum}SP|Q43848|TKTC_SOLTU TRANSKETOLASE, CHLOROP glutamyl-tRNA synthetase {Arabidopsis TC72377 BE461031 cLEG37E10 VID9 T2G18 R7 C7 r4-c2 r1-c3 thaliana}PIR|T52043|T52043 probable glutamate-- tRNA ligase (E URIDYLATE KINASE (EC 2.7.4.—) (UK) (URIDINE TC72400 BE458716 cLEM3K4 VIIID5 T2H10 R15 C8 r4-c2 r1-c3 MONOPHOSPHATE KINASE) (UMP KINASE) (UMP/CMP KINASE).GP| asparagine synthetase {Triphysaria TC72402 AI487482 cLED11G10 IIG10 T1M20 R5 C13 r1-c2 r3-c3 versicolor}GP|2429282|gb|AAD05034.1||AF014056 asparagine synthet cytochrome p450 lxxii hydroxylase) (ge10h) TC72403 BE459772 cLEM8C1 VIIIF2 T2L4 R21 C12 r4-c2 r1-c3 {Catharanthus roseus}SP|Q05047|CP72_CATRO CYTOCHROME P45 cytochrome P450 {Arabidopsis thaliana} TC72404 AW650317 cLEI12N11 IIB10 T1C20 R5 C3 r1-c2 r3-c3 VACUOLAR ATP SYNTHASE SUBUNIT C (EC TC72410 BG643163 cTOF26D14 XIIE10 T3J20 R5 C10 r2-c1 r4-c3 3.6.1.34) (V-ATPASE C SUBUNIT) (VACUOLAR PROTON PUMP C SUBUNIT). phosphoenolpyruvate carboxylase 2 TC72426 BE459547 cLEM7I13 VC3 T2E5 R20 C5 r4-c2 r1-c3 lipoxygenase{circumflex over ( )}{circumflex over ( )}loxc homologue TC72430 AW442155 cLEN21F5 IXC1 T3E1 R24 C5 r2-c1 r4-c3 lipoxygenase{circumflex over ( )}{circumflex over ( )}loxc homologue TC72431 AW738558 cTOD7B10 XVIIIA4 T5A8 R17 C1 r3-c2 r4-c4 succinyl-CoA synthetase, alpha subunit {Arabidopsis TC72435 AW224006 cLEN14M4 XIIA6 T3B12 R13 C2 r2-c1 r4-c3 thaliana} VACUOLAR ATP SYNTHASE SUBUNIT D (EC TC72437 AW624445 cTOB15F12 XVIIA2 T5A3 R22 C1 r3-c2 r4-c4 3.6.1.34) (V-ATPASE D SUBUNIT) (VACUOLAR PROTON PUMP D SUBUNIT). NADPH-cytochrome P450 oxidoreductase (EC 1.—.—.—)- TC72444 BE354227 cTOD9L11 IIF12 T1F24 R1 C6 r1-c2 r3-c3 common tobacco ATP synthase beta subunit TC72461 BE449406 cLHT31M12 XVC3 T4F5 R20 C6 r2-c2 r1-c4 putative sulfite oxidase {Arabidopsis TC72463 BE431431 cLEG1G5 VF11 T2K21 R4 C11 r4-c2 r1-c3 thaliana}GP|6513940|gb|AAF14844.1|AC011664_26|AC011664 sulfit putative homeodomain transcription factor {Arabidopsis TC72471 BE436986 cLEG35I11 VIC6 T2E12 R13 C5 r4-c2 r1-c3 thaliana}PIR|F84565|F84565 probable homeodom NADP-dependent glyceraldehyde-3-phosphate TC72481 AW616527 cLHT11J5 XIVH10 T4O20 R5 C15 r2-c2 r1-c4 dehydrogenase (non-phosphorylating glyceraldehyde 3- phosph WRKY transcription factor Nt-SubD48 {Nicotiana TC72483 AI487657 cLED13K15 IIH8 T1O16 R9 C15 r1-c2 r3-c3 tabacum} putative anthocyanin 5-aromatic acyltransferase TC72484 AW625642 cLEZ16I6 XIVE2 T4I4 R21 C9 r2-c2 r1-c4 {Arabidopsis thaliana}PIR|G84823|G84823 probable an pyruvate dehydrogenase E1 beta subunit isoform 2 {Zea TC72498 AW096554 cLET38N6 XIH1 T3P1 R24 C16 r2-c1 r4-c3 mays} S-adenosylmethionine decarboxylase {Nicotiana TC72506 AW224365 cLEN16L22 IXA8 T3A15 R12 C1 r2-c1 r4-c3 tabacum}PIR|T01934|T01934 adenosylmethionine decarbox NADH-UBIQUINONE OXIDOREDUCTASE 24 KDA TC72512 AI779124 cLES7M17 XIA10 T3B19 R6 C2 r2-c1 r4-c3 SUBUNIT PRECURSOR (EC 1.6.5.3) (EC 1.6.99.3).GP|7269018|emb|C phosphate/phosphoenolpyruvate translocator precursor TC72515 BG132441 cTOE7J1 XVIIG3 T5M5 R20 C13 r3-c2 r4-c4 {Nicotiana tabacum}GP|1778145|gb|AAB40648.1||U putative glucosyltransferase {Arabidopsis TC72520 AW035575 cLEC39D16 IIC11 T1E22 R3 C5 r1-c2 r3-c3 thaliana}PIR|H84870|H84870 probable glucosyltransferase [ pyruvate dehydrogenase TC72539 BF096522 cLEW12E7 XIID8 T3H16 R9 C8 r2-c1 r4-c3 zinc finger transcription factor-like protein {Arabidopsis TC72540 AW621257 cLEX11K20 XIIIB5 T4C9 R16 C3 r2-c2 r1-c4 thaliana}PIR|T49899|T49899 zinc finger t flavanone 3-hydroxylase-like protein {Arabidopsis TC72542 BG133370 cTOE12M9 XVIIIB12 T5C24 R1 3C r3-c2 r4-c4 thaliana} gamma-glutamlcysteine synthetase TC72560 BE432272 cLEG7C8 VIH6 T2O12 R13 C15 r4-c2 r1-c3 transcription initiation factor iib (tfiib) {Glycine TC72566 AI775379 cLER15I4 IXF10 T3K19 R6 C11 r2-c1 r4-c3 max}SP|P48513|TF2B_SOYBN TRANSCRIPTION INITIAT dihydroxy-acid dehydratase {Arabidopsis thaliana} TC72576 BE459380 cLEM6L1 VIIIE4 T2J8 R17 C10 r4-c2 r1-c3 arginine methyltransferase (pam1) {Arabidopsis TC72613 AI486209 cLED5L13 IVA12 T1B24 R1 C2 r1-c2 r3-c3 thaliana}GP|7269850|emb|CAB79709.1||AL161575 arginin N-hydroxycinnamoyl/benzoyltransferase {Ipomoea TC72632 AI777857 cLES3C10 XH2 T3O4 R21 C15 r2-c1 r4-c3 batatas} similar to ATPases associated with various cellular TC72650 AW035993 cLEC33L22 IIA5 T1A10 R15 C1 r1-c2 r3-c3 activites (Pfam: AAA.hmm, score: 230.91) {Arabid putative monosaccharide transporter 1 {Petunia x TC72655 BG140550 cLPP17H17 XVE2 T4J3 R22 C10 r2-c2 r1-c4 hybrida} 78 kDa glucose regulated protein homolog 5 precursor TC72660 AI775845 cLER16B20 IXG3 T3M5 R20 C13 r2-c1 r4-c3 (grp 78-5) (immunoglobulin heavy subunit bindin threonine synthase {Solanum tuberosum} TC72666 BG643425 cTOF27J7 XXA4 T5B8 R17 C2 r3-c2 r4-c4 CONSTANS-like B-box zinc finger protein-like TC72668 AI775819 cLER16N13 IXG10 T3M19 R6 C13 r2-c1 r4-c3 {Arabidopsis thaliana} Identical to ribose-phosphate pyrophosphokinase 2 TC72677 AW651192 cLEI15J16 VIIC7 T2F13 R12 C6 r4-c2 r1-c3 (phosphoribosyl pyrophosphate synthetase 2) (PRSII NADH dehydrogenase {Solanum TC72678 AW041573 cLET10A15 XIB11 T3D21 R4 C4 r2-c1 r4-c3 tuberosum}GP|668987|emb|CAA59063.1||X84320 NADH dehydrogenase {Solanum Similar to gb|Z84386 anthranilate N- TC72703 AW616976 cLHT19A14 XVA8 T4B15 R12 C2 r2-c2 r1-c4 hydroxycinnamoyl/benzoyltransferase from Dianthus caryophyllus. putative H+-transporting ATPase {Oryza sativa} TC72705 AW094623 cLET29G16 IXA4 T3A7 R18 C1 r2-c1 r4-c3 Similar to Populus balsamifera subsp. trichocarpa X TC72708 AW929488 cTOC9G1 XVIIF7 T5K13 R12 C11 r3-c2 r4-c4 Populus deltoides vegetative storage protein. cytochrome P450-dependent fatty acid hydroxylase TC72710 BE433735 cLEG20P11 VG5 T2M9 R16 C13 r4-c2 r1-c3 {Vicia sativa} anthocyanidin 3-O-glucosyltransferase {Petunia x TC72713 AI488786 cLED18F12 IIIB7 T1D13 R12 C4 r1-c2 r3-c3 hybrida} cytochrome p450 lxxia4 {Solanum TC72718 BE431818 cLEG4A21 VIG10 T2M20 R5 C13 r4-c2 r1-c3 melongena}SP|P37117|C714_SOLME CYTOCHROME P450 71A4 (EC 1.14.—.—) ( cytochrome p450 lxxia4 {Solanum TC72719 AI487522 cLED11B9 IIG8 T1M16 R9 C13 r1-c2 r3-c3 melongena}SP|P37117|C714_SOLME CYTOCHROME P450 71A4 (EC 1.14.—.—) ( phosphoenolpyruvate carboxykinase {Flaveria pringlei} TC72722 BE436435 cLEG32K2 VIB1 T2C2 R23 C3 r4-c2 r1-c3 phosphoribosyl pyrophosphate synthase {Spinacia TC72727 AW622719 cTOB4I14 XVIB5 T4D10 R15 C4 r2-c2 r1-c4 oleracea} dehydroquinate dehydratase/shikimato:NADP TC72770 BF051225 cLEM21P8 VIIIA9 T2B18 R7 C2 r4-c2 r1-c3 oxidoreductase AP2 domain containing protein {Prunus armeniaca} TC72775 BG132603 cTOE8E22 XVIIIG3 T5M6 R19 C13 r3-c2 r4-c4 putative phosphate/phosphoenolpyruvate translocator TC72794 BF051658 cLEM23F10 IIH2 T1O4 R21 C15 r1-c2 r3-c3 {Arabidopsis thaliana} SNAP25A protein {Arabidopsis TC72817 AW041561 cLET10A17 XIB12 T3D23 R2 C4 r2-c1 r4-c3 thaliana}GP|5731763|emb|CAB52582.1||X92419 SNAP25A protein {Arabidopsi heat shock transcription factor like protein {Arabidopsis TC72821 AI897308 cLED26B20 IIID7 T1H13 R12 C8 r1-c2 r3-c3 thaliana}GP|2244754|emb|CAB10177.1||Z9733 ADP-glucose pyrophosphorylase large subunit 1 TC72843 BG126269 cTOF11F18 XVIIIG11 T5M22 R3 C13 r3-c2 r4-c4 putative methylmalonate semi-aldehyde dehydrogenase TC72868 BG643765 cTOF32D7 XXC9 T5F18 R7 C6 r3-c2 r4-c4 {Arabidopsis thaliana}PIR|H84514|H84514 hypothe flavonol 3-o-glucosyltransferase 6 {Manihot TC72874 AW031872 cLEC38K2 IIC9 T1E18 R7 C5 r1-c2 r3-c3 esculenta}SP|Q40288|UFO6_MANES FLAVONOL 3- O-GLUCOSYLTRA Identical to gene ZW10 from Arabidopsis thaliana TC72889 AW091993 cLET17D3 XID9 T3H17 R8 C8 r2-c1 r4-c3 gb|AB028195 and is a member of the Phosphoglycerate coproporphyrinogen iii oxidase precursor TC72896 BG125496 cTOF8H12 XXG4 T5N8 R17 C14 r3-c2 r4-c4 (coproporphyrinogenase) (coprogen oxidase) {Nicotiana tabac zinc finger protein-like {Arabidopsis TC72898 AI484751 cLED3B15 IIIH9 T1P17 R8 C16 r1-c2 r3-c3 thaliana}GP|5006473|gb|AAD37511.1|AF139098_1|AF139098 putativ caffeoyl-CoA O-methyltransferase {Nicotiana TC72904 BG133660 cTOE13D5 VIIE4 T2J7 R18 C10 r4-c2 r1-c3 tabacum}GP|1103487|emb|CAA91228.1||Z56282 caffeoyl-CoA phosphoglycerate mutase {Solanum tuberosum} TC72922 AW648021 cLEI3M7 VIIE1 T2J1 R24 C10 r4-c2 r1-c3 acetyl-CoA C-acetyltransferase {Arabidopsis thaliana} TC72945 AW217996 cTOD6E1 VA5 T2A9 R16 C1 r4-c2 r1-c3 acetyl-CoA C-acetyltransferase {Arabidopsis thaliana} TC72946 BG126595 cTOF12F6 XVIIIH4 T5O8 R17 C15 r3-c2 r4-c4 putative NADH-ubiquinone oxireductase {Arabidopsis TC72951 BE431573 cLEG27G1 VG12 T2M23 R2 C13 r4-c2 r1-c3 thaliana}PIR|C84588|C84588 probable NADH-ubiquin acetyl-CoA C-acetyltransferase {Arabidopsis thaliana} TC72956 AI485611 cLED6JI8 IVB9 T1D18 R7 C4 r1-c2 r3-c3 malonyl-CoA:ACP transacylase {Perilla frutescens} TC72961 AW648980 cLEI6N11 XVG1 T4N1 R24 C14 r2-c2 r1-c4 N-carbamyl-L-amino acid amidohydrolase-like protein TC72977 AW649291 cLEI7D16 VIIF8 T2L15 R12 C12 r4-c2 r1-c3 {Arabidopsis thaliana} uracil phosphoribosyltransferase {Nicotiana TC72985 BE458242 cLEM1J11 VIIH10 T2P19 R6 C16 r4-c2 r1-c3 tabacum}SP|P93394|UPP_TOBAC URACIL PHOSPHORIBOSYLTRANSF heat stress transcription factor A3 {Lycopersicon TC72992 AW035854 cLEC36E8 IIB9 T1C18 R7 C3 r1-c2 r3-r3 peruvianum} invertase-like protein {Arabidopsis TC73000 BF114092 cLEY24H5 IVG6 T1N12 R13 C14 r1-c2 r3-c3 thaliana}GP|7270437|emb|CAB80203.1||AL161586 invertase-like pro contains similarity to acyl-CoA TC73001 BE432689 cLEG9J24 VIIA6 T2B11 R14 C2 r4-c2 r1-c3 thioesterase~gene_id: K23F3.9 {Arabidopsis thaliana} acetylornithine aminotransferase precursor {Alnus TC73014 AW650016 cLEI11O22 VIIA12 T2B23 R2 C2 r4-c2 r1-c3 glutinosa}SP|O04866|ARGD_ALNGL ACETYLORNITHINE AM glucose-6-phosphate isomerase {Spinacia TC73016 AW030975 cLEC5G17 IA10 T1A19 R6 C1 r1-c2 r3-c3 oleracea}PIR|T09153|T09153 glucose-6-phosphate isomerase (E hydroxypyruvate reductase {Bruguiera gymnorhiza} TC73027 AW040337 cLET5K21 XIIB11 T3D22 R3 C4 r2-c1 r4-c3 PROTEIN-L-ISOASPARTATE O- TC73037 AW623004 cTOB7N21 XVIIB7 T5C13 R12 C3 r3-c2 r4-c4 METHYLTRANSFERASE (EC 2.1.1.77) (PROTEIN- BETA-ASPARTATE METHYLTRANSFERASE) putative anthocyanidin-3-glucoside TC73055 BE450766 cLEY15C5 XIIIH1 T4O1 R24 C15 r2-c2 r1-c4 rhamnosyltransferase {Arabidopsis thaliana}PIR|D84614|D84614 hyp putative RING-H2 zinc finger protein ATL6 TC73059 BF051368 cLEM22N1 VIIIB5 T2D10 R15 C4 r4-c2 r1-c3 {Arabidopsis thaliana} adenosine kinase {Arabidopsis TC73160 BF113600 cLEY21J1 XIVB9 T4C18 R7 C3 r2-c2 r1-c4 thaliana}GP|7378610|emb|CAB83286.1||AL162751 adenosine kinase-like pr putative PHD-type zinc finger protein {Arabidopsis TC73164 AI775153 cLER14N11 IXF6 T3K11 R14 C11 r2-c1 r4-c3 thaliana}PIR|A84437|A84437 probable PHD-type zin quinolinate phosphoribosyltransferase {Nicotiana TC73169 AI894647 cLEC4L14 XIIA9 T3B18 R7 C2 r2-c1 r4-c3 tabacum} 5-enolpyruvylshikimate-3-phosphate synthase precursor TC73179 AW041710 cLET12G6 XIC8 T3F15 R12 C6 r2-c1 r4-c3 (EC 2.5.1.19) transcription factor TC73183 AI897672 cLED30E23 IIIF1 T1L1 R24 C12 r1-c2 r3-c3 Dof zinc finger protein {Arabidopsis TC73204 AI897222 cLED27I9 IIIE1 T1J1 R24 C10 r1-c2 r3-c3 thaliana}GP|9280230|dbj|BAB01720.1||AB023045 Dof zinc finger p aldose 1-epimerase-like protein {Arabidopsis TC73210 AW441440 cLEN17M15 IXB2 T3C3 R22 C3 r2-c1 r4-c3 thaliana}PIR|T07719|T07719 aldose 1-epimerase homolog glucosyl transferase {Nicotiana TC73225 AI487283 cLED10H21 IIG3 T1M6 R19 C13 r1-c2 r3-c3 tabacum}GP|1805359|dbj|BAA19155.1||AB000623 glucosyl transferase {N unnamed protein product TC73255 AI486456 cLED8C24 IVC7 T1F14 R11 C6 r1-c2 r3-c3 {unidentified}□GP|2462931|emb|CAB06082.1||Z83833 UDP-glucose:sterol glucosyl homogentisate 1,2-dioxygenase TC73262 AW737196 cTOD2I2 XIIA11 T3B22 R3 C2 r2-c1 r4-c3 putative aspartate aminotransferase; 38163-36256 TC73280 AI488655 cLED18H16 IIIB9 T1D17 R8 C4 r1-c2 r3-c3 {Arabidopsis thaliana}PIR|C96835|C96835 hypothetic ATP synthase alpha chain {Vigna radiata} TC73289 BG125450 cTOF8N13 VIE5 T2I10 R15 C9 r4-c2 r1-c3 MYB-like DNA-binding protein {Catharanthus roseus} TC73317 AW039424 cLET12C14 XIC6 T3F11 R14 C6 r2-c1 r4-c3 CYTOCHROME P450 90A1 (EC 1.14.—.—). TC73326 AW648875 cLEI6O5 VIIF7 T2L13 R12 C12 r4-c2 r1-c3 GP|853719|emb|CAA60793.1||X87367 CYP90 protein {Arabidopsis thal vsf-1{circumflex over ( )}{circumflex over ( )}transcription factor VSF-1 TC73332 BE460903 cLEG36J22 VID1 T2G2 R23 C7 r4-c2 r1-c3 ATP synthase alpha subunit {Nicotiana TC73341 AI898491 cLED34M3 IIIG10 T1N19 R6 C14 r1-c2 r3-c3 tabacum}SP|P00823|ATPA_TOBAC ATP SYNTHASE ALPHA CHAIN (EC 3.6 isoflavone reductase homolog {Solanum TC73357 BG124289 cTOF4F20 XXE3 T5J6 R19 C10 r3-c2 r4-c4 tuberosum}SP|P52578|IFRH_SOLTU ISOFLAVONE REDUCTASE HOMOLOG ( fumarase {Solanum TC73367 AW034595 cLEC11N11 IC4 T1E7 R18 C5 r1-c2 r3-c3 tuberosum}GP|1488652|emb|CAA62817.1||X91615 fumarase {Solanum tuberosum}PIR|T073 ornithine carbamoyltransferase; OCTase {Canavalia TC73370 AI486421 cLED5L18 IVB1 T1D2 R23 C4 r1-c2 r3-c3 lineata}GP|12003188|gb|AAG43481.1|AF203688_1|AF20 N-glyceraldehyde-2-phosphotransferase-like TC73374 BG129565 cTOF24P2 XXG12 T5N24 R1 C14 r3-c2 r4-c4 {Arabidopsis thaliana} putative cinnamyl alcohol dehydrogenase {Malus x TC73375 BE437155 cLEG35N3 VIC9 T2E18 R7 C5 r4-c2 r1-c3 domestica}PIR|T16995|T16995 probable cinnamyl-alco putative anthocyanidin-3-glucoside TC73422 AW031678 cLEC37H19 IIC2 T1E4 R21 C5 r1-c2 r3-c3 rhamnosyltransferase {Arabidopsis thaliana}PIR|D84614|D84614 hyp serine/threonine-specific protein kinase NAK TC73426 AI773080 cLER5E14 XB12 T3C24 R1 C3 r2-c1 r4-c3 {Arabidopsis thaliana}PIR|T48250|T48250 serine/threoni putative threonine dehydratase/deaminase {Oryza TC73457 AI897298 cLED26P9 IIID12 T1H23 R2 C8 r1-c2 r3-c3 sativa} pyruvate dehydrogenase kinase {Arabidopsis thaliana} TC73458 AI774213 cLER11N24 IXE5 T3I9 R16 C9 r2-c1 r4-c3 Cytochrome P450-like protein {Arabidopsis TC73461 AW932471 cLEF48M22 IVH12 T1P24 R1 C16 r1-c2 r3-c3 thaliana}GP|7270098|emb|CAB79912.1||AL161580 Cytochrome P putative arginine methyltransferase {Arabidopsis TC73476 AW647829 cLEI2M24 VIID8 T2H15 R12 C8 r4-c2 r1-c3 thaliana} glutamine synthetase {Nicotiana TC73479 BE450846 cLEY15G20 XIIIH4 T4O7 R18 C15 r2-c2 r1-c4 tabacum}GP|1419094|emb|CAA65173.1||X95932 glutamine synthetase {Nic glucosyl transferase {Nicotiana TC73487 BE436515 cLEG32P19 VIB3 T2C6 R19 C3 r4-c2 r1-c3 tabacum}GP|1805359|dbj|BAA19155.1||AB000623 glucosyl transferase {N putative RING zinc finger protein; 36546-35989 TC73490 AW223330 cLEN11H5 VIIIG6 T2N12 R13 C14 r4-c2 r1-c3 {Arabidopsis thaliana}GP|12323975|gb|AAG51946.1|AC01 cytochrome P450 {Nicotiana tabacum} TC73493 BG126018 cTOF10P11 IIF6 T1K12 R13 C11 r1-c2 r3-c3 PHOSPHOGLUCOMUTASE, CYTOPLASMIC (EC TC73495 BF050298 cLEM17E12 XVH5 T4P9 R16 C16 r2-c2 r1-c4 5.4.2.2) (GLUCOSE PHOSPHOMUTASE) (PGM).GP|8250624|emb|CAB93681. starch phosphorylase (AA 1-966) {Solanum tuberosum} TC73506 AW934093 cLEF57H6 VC6 T2E11 R14 C5 r4-c2 r1-c3 alpha-glucan phosphorylase, 1 isozyme 1 precursor TC73507 AW618336 cLPT12G14 XVG3 T4N5 R20 C14 r2-c2 r1-c4 (starch phosphorylase 1-1) {Solanum tuberosum}SP| acetyl-coA dehydrogenase, putative {Arabidopsis TC73523 BF113496 cLEY21I7 XIVB8 T4C16 R9 C3 r2-c2 r1-c4 thaliana} 1-asparaginase (1-asparagine amidohydrolase) TC73526 AW031986 cLEC34N1 IIA11 T1A22 R3 C1 r1-c2 r3-c3 {Arabidopsis thaliana} PROBABLE TC73527 AW223040 cLEN10E2 VIIIG2 T2N4 R21 C14 r4-c2 r1-c3 PHOSPHORIBOSYLFORMYLGLYCINAMIDINE SYNTHASE, CHLOROPLAST PRECURSOR (EC 6.3.5.3) (FGAM SYNTHA Putative phospholipid cytidylyltransferase {Oryza TC73548 AW221069 cLEF3J23 IVF7 T1L14 R11 C12 r1-c2 r3-c3 sativa} 2-oxoglutarate/malate translocator {Arabidopsis TC73585 AW093605 cLET25M14 XIH6 T3P11 R14 C16 r2-c1 r4-c3 thaliana} putative ripening-related bZIP protein {Vitis vinifera} TC73588 AW617938 cLPT11O16 XVG2 T4N3 R22 C14 r2-c2 r1-c4 ethylene-responsive transcriptional coactivator TC73593 BG129027 cTOF23I9 XIXF12 T5L23 R2 C12 r3-c2 r4-c4 PHOSPHOGLUCOMUTASE, CYTOPLASMIC (EC TC73595 AI771994 cLER1I10 XA7 T3A14 R11 C1 r2-c1 r4-c3 5.4.2.2) (GLUCOSE PHOSPHOMUTASE) (PGM).GP|8250624|emb|CAB93681. putative transcripton factor {Nostoc sp. PCC 7120} TC73599 AW034565 cLEC12H20 IC6 T1E11 R14 C5 r1-c2 r3-c3 microsomal oleate desaturase {Arachis ipaensis} TC73604 BG136483 cLPP3E13 XVE10 T4J19 R6 C10 r2-c2 r1-c4 pyruvate dehydrogenase e1 component, alpha subunit TC73607 AW224394 cLEW6P3 XIIH9 T3P18 R7 C16 r2-c1 r4-c3 precursor {Solanum tuberosum}SP|P52903|ODPA_SOLT enoyl-ACP reductase {Nicotiana TC73615 AW622780 cTOB1E5 XVIIA11 T5A21 R4 C1 r3-c2 r4-c4 tabacum}GP|2204236|emb|CAA74176.1||Y13861 enoyl-ACP reductase {Nicot putative dehydroquinase shikimate dehydrogenase TC73630 AW623099 cTOB8G2 XVIIB10 T5C19 R6 C3 r3-c2 r4-c4 {Arabidopsis thaliana} myb-related transcription factor {Lycopersicon TC73643 AI898594 cLED34B18 IIIG4 T1N7 R18 C14 r1-c2 r3-c3 esculentum}PIR|T07393|T07393 myb-related transcripti bZIP transcriptional activator RSG, putative TC73646 AW223726 cLEN12N16 VIIIG10 T2N20 R5 C14 r4-c2 r1-c3 {Arabidopsis thaliana}GP|12321383|gb|AAG50761.1|AC0791 putative zinc finger protein {Oryza sativa} TC73652 BF052197 cLEM25L18 XVG9 T4N17 R8 C14 r2-c2 r1-c4 pyruvate kinase (EC 2.7.1.40) A, chloroplast-common TC73662 AW223671 cLEN12P17 VD2 T2G3 R22 C7 r4-c2 r1-c3 tobacco 6-phosphogluconate dehydrogenase, putative; 13029-14489 TC73678 AI780193 cLES11C1 XD2 T3G4 R21 C7 r2-c1 r4-c3 {Arabidopsis thaliana} zinc-finger protein, putative; 7043-7771 {Arabidopsis TC73679 AW031533 cLEC34F1 XVIC12 T4F24 R1 C6 r2-c2 r1-c4 thaliana}PIR|H86450|H86450 probable zinc-fing ornithine aminotransferase {Arabidopsis thaliana} TC73702 BG642898 cTOF26A17 XIXH3 T5P5 R20 C16 r3-c2 r4-c4 pyrophosphate-dependent phosphofructo-1-kinase TC73706 BE433184 cLEG12J15 VID3 T2G6 R19 C7 r4-c2 r1-c3 {Arabidopsis thaliana}GP|7269478|emb|CAB79482.1||AL1 sugar-phosphate isomerase-like protein {Arabidopsis TC73722 BF113143 cLEG43N9 VIG6 T2M12 R13 C13 r4-c2 r1-c3 thaliana}PIR|T47628|T47628 sugar-phosphate isom cytochrome P450, putative {Arabidopsis thaliana} TC73737 AW624021 cTOB13J12 XVIH7 T4P14 R11 C16 r2-c2 r1-c4 RING-H2 finger protein RHF2a {Arabidopsis TC73753 cLHT23O1 cLHT23O1 IG10 T1M19 R6 C13 r1-c2 r3-c3 thaliana}GP|13374859|emb|CAC34493.1||AL589883 RING-H2 fin Contains similarity to gb|AF136530 transcriptional TC73763 BG124550 cTOF5G18 XXF1 T5L2 R23 C12 r3-c2 r4-c4 regulator from Zea mays. {Arabidopsis thaliana}P glucose-6-phosphate 1-dehydrogenase {Solanum TC73842 AW616687 cLHT12I23 XIVH12 T4O24 R1 C15 r2-c2 r1-c4 tuberosum} putative pyrophosphate--fructose-6-phosphate 1- TC73845 BE462789 cTOA15B6 XVID6 T4H12 R13 C8 r2-c2 r1-c4 phosphotransferase {Arabidopsis thaliana}PIR|B84613| putative glucosyltransferase {Arabidopsis TC73904 AI485027 cLED2F12 IIIE8 T1J15 R12 C10 r1-c2 r3-c3 thaliana}PIR|E84680|E84680 probable glucosyltransferase [ acetyl-CoA synthetase {Solanum tuberosum} TC73927 BG133933 cTOE14H4 XVIIIC5 T5E10 R15 C5 r3-c2 r4-c4 Knotted 1 (TKn1) TC73929 AW648827 cLEI6C17 VIIF2 T2L3 R22 C12 r4-c2 r1-c3 homeotic protein BEL1 homolog {Arabidopsis thaliana} TC73945 BG129460 cTOF24F9 XIXG6 T5N11 R14 C14 r3-c2 r4-c4 flavanone 3-hydroxylase-like protein {Arabidopsis TC73949 AW218877 cLEX1K4 XIIID6 T4G11 R14 C7 r2-c2 r1-c4 thaliana} putative cinnamoyl CoA reductase {Arabidopsis TC73957 BE460616 cLEG33E6 VIB8 T2C16 R9 C3 r4-c2 r1-c3 thaliana}PIR|C84630|C84630 probable cinnamoyl CoA red glucosyl transferase {Nicotiana TC73986 AI898797 cLED35N9 IIIG12 T1N23 R2 C14 r1-c2 r3-c3 tabacum}GP|1805359|dbj|BAA19155.1||AB000623 glucosyl transferase {N helicase-like transcription factor-like protein TC73997 AW093171 cLET23N4 XIF4 T3L7 R18 C12 r2-c1 r4-c3 {Arabidopsis thaliana} pyruvate dehydrogenase E1 beta subunit isoform 1 {Zea TC74002 BE459681 cLEM7B14 VIIIE8 T2J16 R9 C10 r4-c2 r1-c3 mays} fructose-6-phosphate 2-kinase/fructose-2,6- TC74004 AI896936 cLEC24G15 IIF10 T1K20 R5 C11 r1-c2 r3-c3 bisphosphatase {Solanum tuberosum}PIR|T07016|T07016 6-ph 1,4-alpha-glucan branching enzyme {Solanum TC74010 AI484710 cLED3F9 IVA1 T1B2 R23 C2 r1-c2 r3-c3 tuberosum}□GP|1621012|emb|CAA70038.1||Y08786 1,4-alpha-gl 76 kDa mitochondrial complex I subunit {Solanum TC74019 AW096331 cLET38C16 XIG11 T3N21 R4 C14 r2-c1 r4-c3 tuberosum}SP|Q43644|NUAM_SOLTU NADH- UBIQUINONE OXID Similar to ATP-citrate-lyase {Arabidopsis TC74060 BE463260 cTOC12I8 XVIIC7 T5E13 R12 C5 r3-c2 r4-c4 thaliana}PIR|F96633|F96633 hypothetical protein F8A5.32 [ putative anthocyanidin-3-glucoside TC74086 AW625949 cLEZ17N5 XIVE7 T4I14 R11 C9 r2-c2 r1-c4 rhamnosyltransferase {Arabidopsis thaliana}PIR|D84614|D84614 hyp floral homeotic protein pmads 2 {Petunia TC74087 AW929900 cTOC8C8 XVIIE11 T5I21 R4 C9 r3-c2 r4-c4 hybrida}SP|Q07474|MAD2_PETHY FLORAL HOMEOTIC PROTEIN PMADS CYTOCHROME P450 71D10 (EC 1.14.—.—). TC74103 AW648815 cLEI6A3 XIIF5 T3L10 R15 C12 r2-c1 r4-c3 GP|2739000|gb|AAB94588.1||AF022459 CYP71D10p {Glycine max}PIR| putative CONSTANS-like B-box zinc finger protein TC74105 AW617537 cLHT23N13 VB9 T2C17 R8 C3 r4-c2 r1-c3 {Arabidopsis thaliana}PIR|G84920|G84920 hypothetic Similar to gb|X90982 phosphoenolpyruvate carboxylase TC74116 AW738719 cTOD8G6 VB4 T2C7 R18 C3 r4-c2 r1-c3 (ppc1) from Solanum tuberosum. {Arabidopsis tha putative lipoxygenase {Arabidopsis TC74124 AW651422 cLEI16J7 XVIIF6 T5K11 R14 C11 r3-c2 r4-c4 thaliana}PIR|B96699|B96699 probable lipoxygenase F12B7.11 [impor putative beta-amylase {Arabidopsis TC74131 BG643197 cTOF26L2 XIXH10 T5P19 R6 C16 r3-c2 r4-c4 thaliana}GP|5302810|emb|CAB46051.1||Z97342 putative beta-amylase UDP-glucose:protein transglucosylase {Solanum TC74136 AW738238 cTOD5P3 XVIIH11 T5O21 R4 C15 r3-c2 r4-c4 tuberosum} hydroxymethyltransferase {Arabidopsis TC74141 BE450641 cLEY14O16 XIIIG10 T4M19 R6 C13 r2-c2 r1-c4 thaliana}GP|2244749|emb|CAB10172.1||Z97335 hydroxymethyltrans hexose transporter {Nicotiana tabacum} TC74146 AW617271 cLHT22B5 IVF6 T1L12 R13 C12 r1-c2 r3-c3 alpha-glucosidase {Solanum tuberosum subsp. TC74149 AW651564 cLEI17E11 VIID4 T2H7 R18 C8 r4-c2 r1-c3 tuberosum} ATP synthase delta' subunit, mitochondrial precursor TC74166 AI774812 cLER13M16 IXF1 T3K1 R24 C11 r2-c1 r4-c3 {Ipomoea batatas}SP|Q40089|ATP4_IPOBA ATP SYNT knotted1-like homeobox protein {Malus TC74178 AW622767 cTOB1A17 XVIIA8 T5A15 R12 C1 r3-c2 r4-c4 domestica}SP|O04136|HKL3_MALDO HOMEOBOX PROTEIN KNOTTED-1 LIK GLYCINE DEHYDROGENASE TC74186 BG126353 cTOF12G5 XVIIIH5 T5O10 R15 C15 r3-c2 r4-c4 [DECARBOXYLATING], MITOCHONDRIAL PRECURSOR (EC 1.4.4.2) (GLYCINE DECARBOXYLASE contains similarity to CONSTANS TC74187 BG127619 cTOF17G8 XIXB3 T5D5 R20 C4 r3-c2 r4-c4 homologs~gene_id: MIF21.14 {Arabidopsis thaliana} chalcone synthase TC74227 AW617911 cLPT11A16 XXIF2 T6K3 R22 C11 r3-c1 r2-c4 ADP-glucose pyrophosphorylase large subunit TC74234 AW622851 cTOB5H12 XVIIB5 T5C9 R16 C3 r3-c2 r4-c4 aldose 1-epimerase-like protein {Arabidopsis thaliana} TC74239 BG133289 cTOE11N22 XVIIIB10 T5C20 R5 C3 r3-c2 r4-c4 3-phosphoshikimate 1-carboxyvinyltransferase TC74249 AW650241 cLEI12M14 IA5 T1A9 R16 C1 r1-c2 r3-c3 precursor (5-enolpyruvylshikimate-3-phosphate synthase) CYTOCHROME P450 98A2 (EC 1.14.—.—). TC74259 BE450893 cLEY15F17 XIIIH3 T4O5 R20 C15 r2-c2 r1-c4 GP|2738998|gb|AAB94587.1||AF022458 CYP98A2p {Glycine max}PIR|T0 zinc finger protein {Oryza sativa}PIR|JE0113|JE0113 TC74290 BG129164 cTOF23D3 XIXF9 T5L17 R8 C12 r3-c2 r4-c4 zinc-finger protein S3574 [imported]-rice Chain A, Glycolate Oxidase (E.C.1.1.3.15) Mutant With TC74300 AI896203 cLEC14K6 IVG11 T1N22 R3 C14 r1-c2 r3-c3 Tyr 24 Replaced By Phe (Y24f)GP|999543|pdb|1G RING finger-like protein {Arabidopsis TC74308 BE433585 cLEG16I12 VE12 T2I23 R2 C9 r4-c2 r1-c3 thaliana}PIR|T47605|T47605 RING finger-like protein- Arabido Contains similarity to acyl-CoA thioesterase from TC74331 BE462429 cTOA13A1 XVID3 T4H6 R19 C8 r2-c2 r1-c4 Streptomyces coelicolor A3(2) gb|AL163641. EST gb putative bZIP transcription factor {Arabidopsis TC74347 AW224459 cLEW6F7 XVIIA5 T5A9 R16 C1 r3-c2 r4-c4 thaliana}PIR|G84831|G84831 probable bZIP transcript hyoscyamine 6-dioxygenase hydroxylase, putative TC74351 BG629895 cLEL30F24 XXIH5 T6O9 R16 C15 r3-c1 r2-c4 {Arabidopsis thaliana}PIR|G86472|G86472 probable hy leucine zipper transcription factor TGA2.1 {Nicotiana TC74356 BE459991 cLEM8L3 VIIIF7 T2L14 R11 C12 r4-c2 r1-c3 tabacum}SP|O24160|TG21_TOBAC TGACG- SEQUENCE S succinate dehydrogenase flavoprotein alpha subunit TC74365 BG130159 cTOF29O16 XXB4 T5D8 R17 C4 r3-c2 r4-c4 {Arabidopsis thaliana}GP|8843734|dbj|BAA97282.1| cytochrome P450 {Arabidopsis thaliana} TC74397 AW616398 cLHT11A5 XIVG12 T4M24 R1 C13 r2-c2 r1-c4 N-hydroxycinnamoyl/benzoyltransferase-like protein TC74426 BE460983 cLEG37K7 VID11 T2G22 R3 C7 r4-c2 r1-c3 {Arabidopsis thaliana} phosphoribosyl pyrophosphate synthase isozyme 4 TC74427 AW224477 cLEW6J7 XXIG6 T6M11 R14 C13 r3-c1 r2-c4 {Spinacia oleracea} (+)-DELTA-CADINENE SYNTHASE ISOZYME A TC74429 AW030787 cLEC22K16 IE12 T1I23 R2 C9 r1-c2 r3-c3 (EC 4.6.1.11) (D-CADINENE SYNTHASE).GP|1217956|emb|CAA65289.1 contains similarity to apoptosis antagonizing TC74441 AI486615 cLED6M5 IVB12 T1D24 R1 C4 r1-c2 r3-c3 transcription factor~gene_id: MFB13.10 {Arabidopsis tha putative sugar transporter; member of major facilitative TC74458 AW738618 cTOD7P2 XIIE4 T3J8 R17 C10 r2-c1 r4-c3 superfamily; integral membrane protein {Bet 4-alpha-glucanotransferase precursor TC74463 AW737154 cTOD2A10 XVIIG4 T5M7 R18 C13 r3-c2 r4-c4 (disproportionating enzyme) (d-enzyme) {Solanum tuberosum}SP|Q NADH glutamate dehydrogenase {Nicotiana TC74481 BE458856 cLEM4D24 VIIID7 T2H14 R11 C8 r4-c2 r1-c3 plumbaginifolia}SP|O04937|DHEA_NICPL GLUTAMATE DEHYDROGENAS bZIP protein {Arabidopsis thaliana}PIR|T49227|T49227 TC74487 BG135017 cTOE21E23 XVIIIE2 T5I4 R21 C9 r3-c2 r4-c4 bZIP protein-Arabidopsis thaliana zinc-finger protein, putative; 7043-7771 {Arabidopsis TC74525 BF051436 cLEM22N6 VIIIB6 T2D12 R13 C4 r4-c2 r1-c3 thaliana}PIR|H86450|H86450 probable zinc-fing cytochrome P450 {Helianthus tuberosus} TC74527 BG130949 cTOE2A19 XVIIIE11 T5I22 R3 C9 r3-c2 r4-c4 fructose-bisphosphate aldolase, cytoplasmic isozyme 1 TC74553 AI781507 cLES16A23 XVG6 T4N11 R14 C14 r2-c2 r1-c4 {Pisum sativum}SP|P46256|ALF1_PEA FRUCTOSE- BI transcriptional adaptor ADA2b {Arabidopsis thaliana} TC74560 AW648772 cLEI5H16 VIIE12 T2J23 R2 C10 r4-c2 r1-c3 putative oxalyl-CoA decarboxylase {Oryza sativa} TC74622 AW094043 cLET27G5 XXIE11 T6I21 R4 C9 r3-c1 r2-c4 putative UDP-N-acetylglucosamine--N-acetylmuramyl- TC74633 BF112480 cLEG41O24 VIF6 T2K12 R13 C11 r4-c2 r1-c3 (pentapeptide)-pyrophosphoryl-undecaprenol N-acety G-Box binding protein 2 {Catharanthus roseus} TC74645 AW648927 cLEI6D11 VIIF3 T2L5 R20 C12 r4-c2 r1-c3 putative indole-3-glycerol phosphate synthase TC74653 AI490823 cLEB3N3 IB9 T1C17 R8 C3 r1-c2 r3-c3 {Arabidopsis thaliana}PIR|B84457|B84457 probable indo contains similarity to nucleotide sugar epimerases TC74661 BE433127 cLEG12I22 VD12 T2G23 R2 C7 r4-c2 r1-c3 {Arabidopsis thaliana}GP|7267098|emb|CAB80769.1| contains similarity to ATPases associated with various TC74673 BE459682 cLEM7B22 VIIIE9 T2J18 R7 C10 r4-c2 r1-c3 cellular activities (Pfam: AAA.hmm, score: 15 putative dihydrolipoamide succinyltransferase TC74697 BE459191 cLEM5D12 XVH12 T4P23 R2 C16 r2-c2 r1-c4 {Arabidopsis thaliana}GP|7269544|emb|CAB79546.1||AL16 auxin-induced basic helix-loop-helix transcription TC74751 AW929135 cTOC4H22 XVIID10 T5G19 R6 C7 r3-c2 r4-c4 factor, putative {Arabidopsis thaliana}GP|123213 Myb-related transcription factor-like protein TC74758 BF097801 cLEW23B2 XIIG3 T3N6 R19 C14 r2-c1 r4-c3 {Arabidopsis thaliana} contains similarity to enolase- TC74779 AW622435 cLEX15O5 XIIID1 T4G1 R24 C7 r2-c2 r1-c4 phosphatase~gene_id: K19P17.1 {Arabidopsis thaliana} formyl transferase, putative {Arabidopsis TC74804 AW034743 cLEC28G7 IG3 T1M5 R20 C13 r1-c2 r3-c3 thaliana}PIR|H96690|H96690 probable formyl transferase F2 immediate-early salicylate-induced glucosyltransferase TC74808 AI778508 cLES5F19 XH10 T3O20 R5 C15 r2-c1 r4-c3 {Nicotiana tabacum}GP|1685005|gb|AAB36653.1| putative para-aminobenzoate synthase and glutamine TC74821 AW224247 cLEN14P12 IXA3 T3A5 R20 C1 r2-c1 r4-c3 amidotransferase, a bifunctional enzyme {Arabidop alpha-glucosidase {Solanum tuberosum subsp. TC74846 AW096689 cLET39H6 XIH5 T3P9 R16 C16 r2-c1 r4-c3 tuberosum} MADS-box transcription factor FBP4 {Petunia x TC74865 AW223028 cLEN10A24 VIIIF12 T2L24 R1 C12 r4-c2 r1-c3 hybrida} NAD-dependent isocitrate dehydrogenase {Nicotiana TC74889 BG124332 cTOF4N22 XXE8 T5J16 R9 C10 r3-c2 r4-c4 tabacum} cytochrome p450 lxxviia1 {Solanum TC74928 AW399268 cLPT6F18 XVIB9 T4D18 R7 C4 r2-c2 r1-c4 melongena}SP|P37123|C771_SOLME CYTOCHROME P450 77A1 (EC 1.14.—.—) threonine deaminase {Nicotiana attenuata} TC74935 AI781599 cLES16D9 XE8 T3I16 R9 C9 r2-c1 r4-c3 putative fatty acid desaturase/cytochrome b5 fusion TC74979 AI780838 cLES13E10 XD9 T3G18 R7 C7 r2-c1 r4-c3 protein {Arabidopsis thaliana}PIR|A84900|A84900 sugar transporter like protein {Arabidopsis TC74988 BF096665 cLEW13D18 XIID9 T3H18 R7 C8 r2-c1 r4-c3 thaliana}GP|2464913|emb|CAB16808.1||Z99708 sugar transp putative UDP-glucose:glycoprotein glucosyltransferase; TC75003 AI775668 cLER16O15 IXG11 T3M21 R4 C13 r2-c1 r4-c3 101200-91134 {Arabidopsis thaliana}PIR|G9673 putative nucleotide-sugar transporter {Arabidopsis TC75014 AW219953 cLEX6M9 XIIIF4 T4K7 R18 C11 r2-c2 r1-c4 thaliana}PIR|E84509|E84509 probable vanadate res Putative UDP-glucose glucosyltransferase {Arabidopsis TC75032 AW621996 cLEX13P4 XIIIC6 T4E11 R14 C5 r2-c2 r1-c4 thaliana}PIR|H86356|H86356 probable UDP-gluco RING-H2 finger protein RHF2a {Arabidopsis TC75038 AW651478 cLEI16F6 VIIC12 T2F23 R2 C6 r4-c2 r1-c3 thaliana}GP|13374859|emb|CAC34493.1||AL589883 RING-H2 fin reticuline oxidase-like protein {Arabidopsis TC75058 AW036319 cLEE1L12 IVD7 T1H14 R11 C8 r1-c2 r3-c3 thaliana}GP|7268879|emb|CAB79083.1||AL161553 reticulin zinc finger protein-like {Arabidopsis thaliana} TC75079 BG128229 cTOF19M22 XIXC9 T5F17 R8 C6 r3-c2 r4-c4 contains similarity to ATPases associated with various TC75096 BG626509 cLEL13B4 XXIB9 T6C17 R8 C3 r3-c1 r2-c4 cellular activities (Pfam: AAA.hmm, score: 15 contains similarity to phosphoenolpyruvate synthase TC75102 AI778552 cLES5N17 XIA1 T3B1 R24 c2 r2-c1 r4-c3 (ppsA) (GB: AE001056) {Arabidopsis thaliana}PIR| cytochrome P450 {Arabidopsis thaliana} TC75118 AW033748 cLEC29K11 IG11 T1M21 R4 C13 r1-c2 r3-c3 Similar to yeast general negative regulator of TC75146 AW617698 cLHT24C16 XVB6 T4D11 R14 C4 r2-c2 r1-c4 transcription subunit 1 {Arabidopsis thaliana}PIR|G8 putative cytochrome P450 {Oryza TC75173 BF112432 cLEG41G20 VIF3 T2K6 R19 C11 r4-c2 r1-c3 sativa}GP|11761120|dbj|BAB19110.1||AP002839 putative cytochrome P45 nitrite reductase {Capsicum annuum} TC75187 BE451369 cLEY17P24 XIVA7 T4A14 R11 C1 r2-c2 r1-c4 tryptophan synthase beta chain {Arabidopsis thaliana} TC75190 BG628235 cLEL21F5 XXIE6 T6I11 R14 C9 r3-c1 r2-c4 Contains a weak similarity to chalcone--flavonone TC75202 BE450563 cLEY13N12 XIIIG3 T4M5 R20 C13 r2-c2 r1-c4 isomerase from Pueraria lobata GP|Q43056 and conta similar to ATPases associated with various cellular TC75211 BE432530 cLEG8L3 VIH12 T2O24 R1 C15 r4-c2 r1-c3 activites (Pfam: AAA.hmm, score: 230.91) {Arabid UTP-glucose glucosyltransferase {Arabidopsis thaliana} TC75218 BG627392 cLEL17E23 XXID1 T6G1 R24 C7 r3-c1 r2-c4 PROBABLE VACUOLAR ATP SYNTHASE TC75225 AW399611 cLPT8M1 XVIC6 T4F12 R13 C6 r2-c2 r1-c4 SUBUNIT H (EC 3.6.1.34) (V-ATPASE H SUBUNIT) (VACUOLAR PROTON PUMP H flavanone 3-hydroxylase-like protein {Arabidopsis TC75238 BG136323 cLPP2E20 XVE8 T4J15 R12 C10 r2-c2 r1-c4 thaliana} isoflavone reductase-like protein {Arabidopsis TC75240 BG127518 cTOF17H7 XIXB4 T5D7 R18 C4 r3-c2 r4-c4 thaliana}GP|7270404|emb|CAB80171.1||AL161585 isoflav cystathionine beta-lyase {Solanum tuberosum} TC75245 AW442491 cLET41E21 XIH12 T3P23 R2 C16 r2-c1 r4-c3 putative acyl-CoA synthetase; 62297-59022 TC75253 BF051331 cLEM22D11 VIIIA11 T2B22 R3 C2 r4-c2 r1-c3 {Arabidopsis thaliana}PIR|D96805|D96805 probable acyl-CoA PHOSPHOGLUCOMUTASE, CHLOROPLAST TC75272 AI484186 cLER1G13 XA6 T3A12 R13 C1 r2-c1 r4-c3 PRECURSOR (EC 5.4.2.2) (GLUCOSE PHOSPHOMUTASE) (PGM).GP|8250622|emb putative cytochrome P450 {Solanum TC75279 AW616142 cLHT6I17 XVC11 T4F21 R4 C6 r2-c2 r1-c4 chacoense}SP|P93531|C7D7_SOLCH CYTOCHROME P450 71D7 (EC 1.14.—.—) hydroxymethyltransferase {Arabidopsis TC75281 AW220206 cLEX9B18 XIIIF8 T4K15 R12 C11 r2-c2 r1-c4 thaliana}GP|2244749|emb|CAB10172.1||Z97335 hydroxymethyltrans cytochrome P450, putative {Arabidopsis TC75284 AI773792 cLER8M23 XC9 T3E18 R7 C5 r2-c1 r4-c3 thaliana}PIR|F86441|F86441 probable cytochrome P450 (importe HD-Zip protein {Arabidopsis TC75348 BG128856 cTOF22F23 XIXE11 T5J21 R4 C10 r3-c2 r4-c4 thaliana}GP|3132474|gb|AAC16263.1||AC003096 homeodomain transcription f putative bZIP transcription factor {Arabidopsis TC75368 BF098455 cLEW27E14 XIIH3 T3P6 R19 C16 r2-c1 r4-c3 thaliana}PIR|G84831|G84831 probable bZIP transcript putative phosphate/phosphoenolpyruvate translocator TC75371 AW617774 cLHT24B5 XVB5 T4D9 R16 C4 r2-c2 r1-c4 protein {Arabidopsis thaliana}PIR|D84649|D84649 myb-like protein {Arabidopsis TC75389 AW224023 cLEN14B1 VIIIH12 T2P24 R1 C16 r4-c2 r1-c3 thaliana}PIR|T48253|T48253 myb-like protein- Arabidopsis thaliana putative glucosyltransferase {Arabidopsis TC75393 BE463368 cTOC12J20 XVIIC8 T5E15 R12 C5 r3-c2 r4-c4 thaliana}PIR|H84786|H84786 probable glucosyltransferase [ tyrosine decarboxylase {Papaver TC75404 AW398822 cLPT5E15 XVIB2 T4D4 R21 C4 r2-c2 r1-c4 somniferum}SP|P54771|TYD5_PAPSO TYROSINE/DOPA DECARBOXYLASE 5 [INCL Similar to gb|U44028 transcription factor CKC from TC75426 GAA824963 CT247 XVIC10 T4F20 R5 C6 r2-c2 r1-c4 Arabidopsis thaliana and contains two PF|00847 AP bZIP transcription factor 6 {Phaseolus vulgaris} TC75472 AW933325 cLEF52N9 VB6 T2C11 R14 C3 r4-c2 r1-c3 HEAT SHOCK FACTOR PROTEIN 7 (HSF 7) (HEAT TC75476 AW931781 cLEF46E16 IVG10 T1N20 R5 C14 r1-c2 r3-c3 SHOCK TRANSCRIPTION FACTOR 7) (HSTF 7).GP|4539457|emb|CAB phosphoenolpyruvate carboxylase 1 {Gossypium TC75495 AW738428 cTOD7E6 XVIIIA5 T5A10 R15 C1 r3-c2 r4-c4 hirsutum}GP|2266947|gb|AAB80714.1||AF008939 phosphoeno CYP82C1p {Glycine max}PIR|T05942|T05942 TC75545 AW039537 cLET14I9 VC12 T2E23 R2 C5 r4-c2 r1-c3 cytochrome P450 82C1-soybean glucose-6-phosphate isomerase {Spinacia TC75577 AW621176 cLEX11E13 XIIIB1 T4C1 R24 C3 r2-c2 r1-c4 oleracea}PIR|T09153|T09153 glucose-6-phosphate isomerase (E cytochrome P450 {Solanum tuberosum} TC75602 BF176446 cLEZ20B13 XIVF11 T4K22 R3 C11 r2-c2 r1-c4 acetyl-CoA synthetase-like protein {Arabidopsis TC75606 BG630353 cLEL35F12 XXIIA4 T6A8 R17 C1 r3-c1 r2-c4 thaliana} Similar to ribokinase {Arabidopsis TC75622 AW933452 cLEF55G23 VB11 T2C21 R4 C3 r4-c2 r1-c3 thaliana}PIR|F86307|F86307 hypothetical protein AAD50017.1 [impo 3-phosphoshikimate 1-carboxyvinyltransferase TC75646 AI487775 cLED10P21 IIG4 T1M8 R17 C13 r1-c2 r3-c3 precursor (5-enolpyruvylshikimate-3-phosphate synthase) TRYPTOPHAN SYNTHASE BETA CHAIN 2 TC75671 AW160221 cLPT1G17 XVH6 T4P11 R14 C16 r2-c2 r1-c4 PRECURSOR (EC 4.2.1.20).GP|2792520|gb|AAB97087.1||AF042320 tryptop cinnamoyl CoA reductase-like protein {Arabidopsis TC75675 AW039131 cLET8J13 XIIC11 T3F22 R3 C6 r2-c1 r4-c3 thaliana}PIR|T48643|T48643 cinnamoyl CoA reductas nucleotide diphosphate kinase Ia {Arabidopsis TC75705 BG124009 cTOF3J14 XXD10 T5H20 R5 C8 r3-c2 r4-c4 thaliana}GP|6065740|emb|CAB58230.1||AJ012758 nucleoti diacylglycerol kinase ATDGK1 homolog {Arabidopsis TC75708 AW737503 cTOD3M20 XVIIG12 T5M23 R2 C13 r3-c2 r4-c4 thaliana}GP|6562306|emb|CAB62604.1||AL133421 diac adenosine kinase {Arabidopsis TC75729 BG129426 cTOF24K12 XIXG8 T5N15 R12 C14 r3-c2 r4-c4 thaliana}GP|7378610|emb|CAB83286.1||AL162751 adenosine kinase-like pr bZIP protein {Arabidopsis thaliana}PIR|T49227|T49227 TC75747 BG135017 cTOE21E23 XVIA7 T4B14 R11 C2 r2-c2 r1-c4 bZIP protein-Arabidopsis thaliana transcription factor like protein {Arabidopsis TC75876 AI484089 cLED25G21 IIID6 T1H11 R14 C8 r1-c2 r3-c3 thaliana}GP|2244999|emb|CAB10419.1||Z97341 transcrip putative RING zinc finger protein {Arabidopsis TC75892 AW931852 cLEF46D13 IVG9 T1N18 R7 C14 r1-c2 r3-c3 thaliana}GP|6682260|gb|AAF23312.1|AC016661_37|AC0166 polyneuridine aldehyde esterase, putative; 10297-12282 TC75906 BG643086 cTOF26F13 XIXH6 T5P11 R14 C16 r3-c2 r4-c4 {Arabidopsis thaliana} glucose 6 phosphate/phosphate translocator-like protein TC75908 AI772836 cLER4C12 XB11 T3C22 R23 C2 r2-c1 r4-c3 {Arabidopsis thaliana}PIR|T51467|T51467 glu leucine zipper transcription factor {Solanum TC75947 AW219193 cLEX3E16 XIIID11 T4G21 R4 C7 r2-c2 r1-c4 tuberosum}GP|575418|emb|CAA57894.1||X82544 leucine zip zinc finger protein-like {Arabidopsis thaliana} TC75949 AW221908 cLEN6G5 IXD3 T3G5 R20 C7 r2-c1 r4-c3 Strong similarity to the TATA binding protein- TC76006 AI490486 cLED20L11 IIIC2 T1F3 R22 C6 r1-c2 r3-c3 associated factor from A. thaliana gb|Y13673. ESTs gb contains similarity to transcription TC76014 AI896705 cLEC22E15 IE10 T1I19 R6 C9 r1-c2 r3-c3 regulator~gene_id: MRG7.19 {Arabidopsis thaliana} putative beta-amylase {Oryza TC76034 AI774687 cLER13G1 IXE11 T3I21 R4 C9 r2-c1 r4-c3 sativa}GP|13489165|gb|AAK27799.1|AC022457_2|AC022457 putative beta-amy aspartate carbamoyltransferase-poj TC76045 phosphate/phosphoenolpyruvate translocator protein- TC76052 BF112541 cLEG41L23 VIF4 T2K8 R17 C11 r4-c2 r1-c3 like {Arabidopsis thaliana} bZIP transcriptional activator RSG {Nicotiana tabacum} TC76055 AI895167 cLEC6P24 IIE12 T1I24 R1 C9 r1-c2 r3-c3 soluble starch (bacterial glycogen) synthase {Solanum TC76060 BF113316 cLEG44E24 VIG8 T2M16 R9 C13 r4-c2 r1-c3 tuberosum}SP|P93568|UGS2_SOLTU SOLUBLE GLYCOG RING zinc finger protein-like {Arabidopsis thaliana} TC76080 AW220356 cLEX10N23 XIIIA10 T4A19 R6 C1 r2-c2 r1-c4 lipoxygenase {Zantedeschia aethiopica} TC76090 AW216452 cLEC85F21 IIF5 T1K10 R15 C11 r1-c2 r3-c3 13-lipoxygenase {Solanum TC76097 AI780011 cLES9J20 XIB8 T3D15 R12 C4 r2-c1 r4-c3 tuberosum}GP|1495802|emb|CAA65268.1||X96405 13- lipoxygenase {Solanum tuber phosphoribosylanthranilate isomerase {Arabidopsis TC76109 AW441506 cLEN17O18 IXB4 T3C7 R18 C3 r2-c1 r4-c3 thaliana} glycine hydroxymethyltransferase (EC 2.1.2.1)-like TC76133 AI782607 cLES20I19 XG7 T3M14 R11 C13 r2-c1 r4-c3 protein {Arabidopsis thaliana}GP|7270156|emb|CAB aldose 1-epimerase-like protein {Arabidopsis thaliana} TC76138 AW218619 cLEZ10I24 XIVC12 T4E24 R1 C5 r2-c2 r1-c4 Contains a bZIP transcription factor PF|00170 domain. TC76171 AI778643 cLES5P4 XIA2 T3B3 R22 C2 r2-c1 r4-c3 ESTs gb|R30400, gb|AA650964, gb|AI994521 come branched-chain alpha-keto acid decarboxylase E1 beta TC76174 BG123833 cTOF3E12 XXD8 T5H16 R9 C8 r3-c2 r4-c4 subunit {Arabidopsis thaliana}PIR|D96597|D9659 HYDROXYMETHYLGLUTARYL-COA SYNTHASE TC76206 AI897702 cLED30M1 XIIH12 T3P24 R1 C16 r2-c1 r4-c3 (EC 4.1.3.5) (HMG-COA SYNTHASE) (3- HYDROXY-3-METHYLGLUTARYL COENZ PROBABLE (S)-2-HYDROXY-ACID OXIDASE, TC76210 AI484731 cLED3B19 IIIH10 T1P19 R6 C16 r1-c2 r3-c3 PEROXISOMAL 2 (EC 1.1.3.15) (GLYCOLATE OXIDASE 2) (GOX 2) (SHOR glycolate oxidase TC76211 AW040933 cLET7O20 XIIC7 T3F14 R11 C6 r2-c1 r4-c3 s-adenosylmethionine decarboxylase proenzyme TC76213 BE450610 cLEY14G24 XIIIG6 T4M11 R14 C13 r2-c2 r1-c4 (induced stolen tip protein tub13) {Solanum tuberosum} S-adenosyl-L-methionine synthetase TC76214 AW650285 cLEI12H5 VIIB2 T2D3 R22 C4 r4-c2 r1-c3 lipoxygenase TC76225 AW441863 cLEN18D8 IXB7 T3C13 R12 C3 r2-c1 r4-c3 lipoxygenase (LOX) TC76226 AW222683 cLEN9C23 IXD11 T3G21 R4 C7 r2-c1 r4-c3 Contains PF|00249 Myb-like DNA-binding domain. TC76257 BE435655 cLEG28A4 VH4 T2O7 R18 C15 r4-c2 r1-c3 EST gb|Z18152 comes from this gene. {Arabidopsis tha UDP-glucose pyrophosphorylase precursor {Solanum TC76266 BF050633 cLEM19E21 VIIH5 T2P9 R16 C16 r4-c2 r1-c3 tuberosum}PIR|JX0128|XNPOU UTP-glucose-1- phosphat hydroxycinnamoyl-CoA:tyramine N- TC76267 AI89443 cLEC4A12 IID9 T1G18 R7 C7 r1-c2 r3-c3 (hydroxycinnamoyl)transferase {Capsicum annuum} hydroxycinnamoyl-CoA:tyramine N- TC76268 AW034593 cLEC11P7 IC5 T1E9 R16 C5 r1-c2 r3-c3 (hydroxycinnamoyl)transferase {Capsicum annuum} hydroxycinnamoyl-CoA:tyramine N- TC76269 AI779165 cLES7G2 XIA7 T3B13 R12 C2 r2-c1 r4-c3 (hydroxycinnamoyl)transferase {Capsicum annuum} hydroxycinnamoyl-CoA:tyramine N- TC76270 AI775716 cLER16I14 IXG7 T3M13 R12 C13 r2-c1 r4-c3 (hydroxycinnamoyl)transferase {Capsicum annuum} tyramine hydroxycinnamoyltransferase {Nicotiana TC76271 AW626294 cLEZ19G14 XIVF5 T4K10 R15 C11 r2-c2 r1-c4 tabacum} tyramine hydroxycinnamoyltransferase {Nicotiana TC76272 AI775105 cLER14F7 XIIA10 T3B20 R5 C2 r2-c1 r4-c3 tabacum} putative transcription factor BTF3 (RNA polymerase B TC76286 BG129308 cTOF23N20 XIXG4 T5N7 R18 C14 r3-c2 r4-c4 transcription factor 3); 26343-27201 {Arabidops putative transcription factor BTF3 (RNA polymerase B TC76287 AW031103 cLEC13K9 ID2 T1G3 R22 C7 r1-c2 r3-c3 transcription factor 3); 26343-27201 {Arabidops chloroplast triose phosphate translocator precursor (ctpt) TC76288 BG127183 cTOF14N1 XIXA4 T5B7 R18 C2 r3-c2 r4-c4 (e29) {Solanum tuberosum}SP|P29463|CPTR_(—) chloroplast triose phosphate translocator precursor (ctpt) TC76289 AW093406 cLET24D14 XIF10 T3L19 R6 C12 r2-c1 r4-c3 (e29) {Solanum tuberosum}SP|P29463|CPTR_(—) anthocyanin 5-O-glucosyltransferase {Petunia x TC76292 AI779099 cLES7I9 XIA9 T3B17 R8 C2 r2-c1 r4-c3 hybrida} phosphoglycerate kinase, cytosolic {Nicotiana TC76300 BG128272 cTOF19H13 XIXC7 T5F13 R12 C6 r3-c2 r4-c4 tabacum}SP|Q42962|PGKY_TOBAC PHOSPHOGLYCERATE KINASE, homeobox 1 protein{circumflex over ( )}{circumflex over ( )}class II knotted-like TC76313 BE436744 cLEG34E19 VIC1 T2E2 R23 C5 r4-c2 r1-c3 homeodomain protein chorismate synthase 1 TC76324 AW626279 cLEZ19C2 XIVF3 T4K6 R19 C11 r2-c2 r1-c4 chorismate synthase 1 precursor 3-phosphate TC76325 BG643072 cTOF26D9 XIXH4 T5P7 R18 C16 r3-c2 r4-c4 phospholyase 1) {Lycopersicon esculentum}SP|Q42884|ARC1 chorismate synthase 1 precursor 3-phosphate TC76326 AI488071 cLED20E15 IIIB12 T1D23 R2 C4 r1-c2 r3-c3 phospholyase 1) {Lycopersicon esculentum}SP|Q42884|ARC1 cytosolic NADP-malic enzyme{circumflex over ( )}{circumflex over ( )}malate dehydrogenase TC76336 AW649636 cLEI8P8 VIIG4 T2N7 R18 C14 r4-c2 r1-c3 ATP synthase gamma subunit, chloroplast precursor TC76348 AI775755 cLER16B11 IXG2 T3M3 R22 C13 r2-c1 r4-c3 {Nicotiana tabacum}SP|P29790|ATPG_TOBAC ATP SYNTH zinc-finger protein {Petunia × TC76350 BE435119 cLEG25I19 VG8 T2M15 R12 C13 r4-c2 r1-c3 hybrida}GP|439493|dbj|BAA05079.1||D26086 zinc- finger protein {Petuni fructokinase TC76354 BE459351 cLEM6F5 VIIIE3 T2J6 R19 C10 r4-c2 r1-c3 ATP synthase beta subunit, mitochondrial precursor TC76359 BE354286 cTOD9H12 XVIIIB7 T5C14 R11 C3 r3-c2 r4-c4 {Nicotiana plumbaginifolia}SP|P17614|ATP2_NICPL spermidine synthase TC76360 AW222198 cLEN7C24 IVG3 T1N6 R19 C14 r1-c2 r3-c3 cDNA~Strawberry pyruvate decarboxylase {Fragaria x TC76372 AI896062 cLEC13B10 IC7 T1E13 R12 C5 r1-c2 r3-c3 ananassa}GP|10121330|gb|AAG13131.1|AF193791_1|AF oxoglutarate malate translocator {Solanum TC76379 BG134301 cLET20P12 XIF2 T3L3 R22 C12 r2-c1 r4-c3 tuberosum}GP|1486472|emb|CAA68164.1||X99853 oxoglutarate aspartate aminotransferase glyoxysomal isozyme AAT1 TC76380 AW029827 cLEC15H12 XIIB1 T3D2 R23 C4 r2-c1 r4-c3 precursor {Glycine max}PIR|T06136|T06136 aspart putative bZIP DNA-binding protein {Capsicum TC76385 BG126538 cTOF12J15 XVIIIH7 T5O14 R11 C15 r3-c2 r4-c4 chinense} ATP synthase B' subunit precursor {Spinacia TC76386 BG123713 cTOF2J20 XXB7 T5D14 R11 C4 r3-c2 r4-c4 oleracea}SP|P31853|ATPX_SPIOL ATP SYNTHASE B' CHAIN PRE ATP synthase beta chain precursor (subunit II) TC76387 AI775445 cLER15F23 XXIH11 T6O21 R4 C15 r3-c1 r2-c4 {Arabidopsis thaliana}GP|2864617|emb|CAA16964.1||AL0 homeodomain-leucine zipper protein 57 {Glycine max} TC76389 AI485338 cLED7K14 IVC5 T1F10 R15 C6 r1-c2 r3-c3 VACUOLAR ATP SYNTHASE SUBUNIT G 1 (EC TC76393 AW222172 cLEN7O7 IVD11 T1H22 R3 C8 r1-c2 r3-c3 3.6.1.34) (V-ATPASE G SUBUNIT 1) (VACUOLAR PROTON PUMP G SUBUN cytochrome p450 1xxii hydroxylase) (ge10h) TC76404 AW030204 cLEC19P18 ID12 T1G23 R2 C7 r1-c2 r3-c3 {Catharanthus roseus}SP|Q05047|CP72_CATRO CYTOCHROME P45 nucleoside diphosphate kinase {Pisum sativum} TC76406 AW626159 cLEZ18D16 XIVE9 T4I18 R7 C9 r2-c2 r1-c4 proline oxidase precursor {Arabidopsis thaliana} TC76411 AW034201 cLEC33G2 IIA2 T1A4 R21 C1 r1-c2 r3-c3 UDP-glucose dehydrogenase {Glycine TC76434 AW648929 cLEI6D15 VIIF4 T2L7 R18 C12 r4-c2 r1-c3 max}SP|Q96558|UGDH_SOYBN UDP-GLUCOSE 6- DEHYDROGENASE (EC 1.1.1.2 UDP-glucose dehydrogenase {Arabidopsis thaliana} TC76435 BE353739 cTOD5J6 IIF7 T1K14 R11 C11 r1-c2 r3-c3 UDP-glucose dehydrogenase-like protein {Arabidopsis TC76436 AW626165 cLEZ18F6 XIVE11 T4I22 R3 C9 r2-c2 r1-c4 thaliana}PIR|T51527|T51527 UDP-glucose dehydrog lipoxygenase {Solanum TC76460 AW030773 cLEC25F7 IF8 TIK15 R12 C11 r1-c2 r3-c3 tuberosum}GP|1407705|gb|AAB67865.1||U60202 lipoxygenase {Solanum tuberosum}P 3-ketoacyl-CoA thiolase {Arabidopsis TC76465 AW037869 cLET3G1 XVIIIB6 T5C12 R13 C3 r3-c2 r4-c4 thaliana}GP|2981618|dbj|BAA25249.1||AB008855 3- ketoacyl-CoA th alanine aminotransferase {Arabidopsis TC76487 AW033411 cLEC28J11 IG5 T1M9 R16 C13 r1-c2 r3-c3 thaliana}GP|12325273|gb|AAG52580.1|AC016529_11| AC016529 putat malate synthase, glyoxysomal {Cucumis TC76489 AW651326 cLEI16E8 VIIC11 T2F21 R4 C6 r4-c2 r1-c3 sativus}SP|P08216|MASY_CUCSA MALATE SYNTHASE, GLYOXYSOMAL (EC putative 6-phosphogluconolactonase {Arabidopsis TC76497 BG133253 cTOE11H12 XVIIIB9 T5C18 R7 C3 r3-c2 r4-c4 thaliana} 6-phosphogluconolactonase-like protein {Arabidopsis TC76498 AW219335 cLEX4G17 XIIIE6 T4I11 R14 C9 r2-c2 r1-c4 thaliana} putative cinnamyl alcohol dehydrogenase {Malus x TC76501 AW096395 cLET38O18 XIH2 T3P3 R22 C16 r2-c1 r4-c3 domestica}PIR|T16995|T16995 probable cinnamyl-alco pyrophosphate-fructose 6-phosphate 1- TC76514 BF097042 cLEW19M9 XIIE9 T3J18 R7 C10 r2-c1 r4-c3 phosphotransferase alpha subunit (pfp) (6- phosphofructokinase pyrophosphate--fructose 6-phosphate 1- TC76515 BE460061 cLEM8H22 VIIIF4 T2L8 R17 C12 r4-c2 r1-c3 phosphotransferase alpha subunit (pfp) (6- phosphofructokinase triosephosphate isomerase chloroplast precursor TC76528 BG133344 cTOE12G21 XIIB4 T3D8 R17 C4 r2-c1 r4-c3 {Spinacia oleracea}SP|P48496|TPIC_SPIOL TRIOSEPHOSP MALATE DEHYDROGENASE [NADP], TC76554 BG129853 cTOF28F11 XXA9 T5B18 R7 C2 r3-c2 r4-c4 CHLOROPLAST PRECURSOR (EC 1.1.1.82) (NADP- MDH).GP|2827076|gb|AAB99753. succinyl-CoA-ligase beta subunit {Arabidopsis TC76558 BG123463 cTOF2C9 XVIF7 T4L14 R11 C12 r2-c2 r1-c4 thaliana}GP|6598664|gb|AAD25643.2|AC007109_1|AC007109 caffeoyl-CoA O-methyltransferase 5 {Nicotiana TC76559 BE450770 cLEY15E1 XIIIH2 T4O3 R22 C15 r2-c2 r1-c4 tabacum}GP|1679853|emb|CAB05369.1||Z82982 caffeoyl-Co fructokinase, putative {Arabidopsis TC76564 BE460923 cLEG36N20 VID4 T2G8 R17 C7 r4-c2 r1-c3 thaliana}GP|12324405|gb|AAG52172.1|AC020665_17| AC020665 fructok transcription factor TEIL {Nicotiana tabacum} TC76569 BF098555 cLEW27J14 XIIH6 T3P12 R13 C16 r2-c1 r4-c3 putative phospholipid cytidylyltransferase {Arabidopsis TC76594 AW031599 cLEC34I4 IIA9 T1A18 R7 C1 r1-c2 r3-c3 thaliana}PIR|H84807|H84807 probable phospho S-adenosylmethionine: 2-demethylmenaquinone TC76601 BG642944 cTOF26K3 XIXH9 T5P17 R8 C16 r3-c2 r4-c4 methyltransferase-like protein {Arabidopsis thaliana} fructose-1,6-bisphosphatase precursor {Solanum TC76605 AW091821 cLET16DB XID6 T3H11 R14 C8 r2-c1 r4-c3 tuberosum} Similar to gb|D86180 phosphoribosylanthranilate TC76611 AW092411 cLET20K18 XIE12 T3J23 R2 C10 r2-c1 r4-c3 transferase from Pisum sativum and contains 2 PF|001 VACUOLAR ATP SYNTHASE 16 KDA TC76632 BG128625 cTOF21F21 XIXE2 T5J3 R22 C10 r3-c2 r4-c4 PROTEOLIPID SUBUNIT (EC 3.6.1.34) (V-ATPASE 16 KDA PROTEOLIPID SUBUNIT glutamate 1-semialdehyde 2,1-aminomutase TC76649 AW039253 cLET8F12 XIIC8 T3F16 R9 C6 r2-c1 r4-c3 FRUCTOSE-1,6-BISPHOSPHATASE, TC76659 BG128167 cTOF19A20 XIXC3 T5F5 R20 C6 r3-c2 r4-c4 CHLOROPLAST PRECURSOR (EC 3.1.3.11) (D- FRUCTOSE-1,6-BISPHOSPHATE 1-PHOS Similar to transaldolase {Arabidopsis TC76672 BG130627 cTOF31N1 XXC7 T5F14 R11 C6 r3-c2 r4-c4 thaliana}PIR|D86257|D86257 hypothetical protein [imported] - CYP94A1 {Vicia sativa}PIR|T08014|T08014 TC76678 AW626091 cLEZ18E2 XIVE10 T4I20 R5 C9 r2-c2 r1-c4 cytochrome P450 CYP94A1-spring vetch 2-isopropylmalate synthase {Lycopersicon TC76694 BF051054 cLEM21M20 VIIIA7 T2B14 R11 C2 r4-c2 r1-c3 pennellii}SP|O04973|LU1A_LYCPN 2- ISOPROPYLMALATE SYNTHASE putative cinnamoyl-CoA reductase {Arabidopsis TC76707 BG130999 cTOE2K3 XVIIIF2 T5K4 R21 C11 r3-c2 r4-c4 thaliana}PIR|D84747|D84747 probable cinnamoyl-CoA red putative nucleotide-sugar dehydratase {Arabidopsis TC76708 AW218947 cLEX2K19 XIIID9 T4G17 R8 C7 r2-c2 r1-c4 thaliana}PIR|T00419|T00419 dTDP-glucose 4-6-dehy zinc finger protein {Arabidopsis thaliana} TC76725 BG125170 cTOF7H24 XXF9 T5L18 R7 C12 r3-c2 r4-c4 transcription factor Hap5a-like protein {Arabidopsis TC76772 BE460825 cLEG36J5 VID2 T2G4 R21 C7 r4-c2 r1-c3 thaliana} cytochrome c oxidase subunit 6b-1 {Oryza TC76784 AW218304 cLEZ6K17 XIVG4 T4M8 R17 C13 r2-c2 r1-c4 sativa}GP|9967277|dbj|BAB12338.1||AB047975 cytochrome c ox beta-fructofuranosidase (invertase){circumflex over ( )}{circumflex over ( )}beta- TC76785 AI486242 cLED5P21 IVB3 T1D6 R19 C4 r1-c2 r3-c3 fructosidase{circumflex over ( )}{circumflex over ( )}beta fructosidase ATP synthase delta subunit, chloroplast precursor TC76808 AI776862 cLER20E5 XVIH4 T4P8 R17 C16 r2-c2 r1-c4 {Nicotiana tabacum}SP|P32980|ATPD_TOBAC ATP SYNTH aminotransferase-like protein {Arabidopsis thaliana} TC76819 BF052130 cLEM25N13 VIIIC11 T2F22 R3 C6 r4-c2 r1-c3 contains similarity to C2H2-type zinc finger TC76821 BE459738 cLEM7L20 VIIIE11 T2J22 R3 C10 r4-c2 r1-c3 protein~gene_id: MOK16.6 {Arabidopsis thaliana} NADH-cytochrome b5 reductase {Arabidopsis TC76827 AW626229 cLEZ19A19 XIVF1 T4K2 R23 C11 r2-c2 r1-c4 thaliana}GP|4240118|dbj|BAA74838.1||AB007800 NADH-cytochr lipoxygenase TC76842 AW035972 cLEC33J22 IIA4 T1A8 R17 C1 r1-c2 r3-c3 Similar to dTDP-D-glucose 4,6-dehydratase TC76851 AW929920 cTOC8G22 XVIIF1 T5K1 R24 C11 r3-c2 r4-c4 {Arabidopsis thaliana}PIR|C96814|C96814 hypothetical prot UDP-glucose: salicylic acid glucosyltransferase TC76866 BE431755 cLEG1L22 VF12 T2K23 R2 C11 r4-c2 r1-c3 {Nicotiana tabacum} putative cytochrome P450 {Arabidopsis TC76887 AW221681 cLEN3H3 IXC7 T3E13 R12 C5 r2-c1 r4-c3 thaliana}GP|13877669|gb|AAK43912.1|AF370593_1|AF370593 putati contains similarity to shikimate kinase TC76889 BG128905 cTOF22P21 XIXF4 T5L7 R18 C12 r3-c2 r4-c4 precursor~gene_id: MDJ14.24 {Arabidopsis thaliana} contains similarity to RING zinc finger TC76902 AW625867 cLEZ17K21 XIVE4 T4I8 R17 C9 r2-c2 r1-c4 protein~gene_id: MBD2.14 {Arabidopsis thaliana} alpha-glucan phosphorylase, h isozyme phosphorylase TC76936 BG129281 cTOF23H24 XVG4 T4N7 R18 C14 r2-c2 r1-c4 h) {Solanum tuberosum}SP|P32811|PHSH_SOLTU ALPH CTP: phosphocholine cytidylyltransferase {Brassica TC76939 AI484842 cLED2N18 IIIE10 T1J19 R6 C10 r1-c2 r3-c3 hapus}GP|1416514|dbj|BAA09644.1||D63168 CTP:phosp citrate synthase {Nicotiana TC76947 AI778988 cLES6D20 XIIA12 T3B24 R1 C2 r2-c1 r4-c3 tabacum}EGAD|126596|143593 citrate synthase {Nicotiana tabacum}GP|2300 nucleoside diphosphate kinase II precursor {Spinacia TC76957 BG128139 cTOF19K9 XIXC8 T5F15 R12 C6 r3-c2 r4-c4 oleracea}SP|Q01402|NDK2_SPIOL NUCLEOSIDE DIPHO delta 1-pyrroline-5-carboxylate synthetase TC76960 BG130959 cTOE2C17 XVIIIE12 T5I24 R1 C9 r3-c2 r4-c4 ferritin subunit cowpea2 precursor {Vigna TC76962 BG134968 cTOE20L1 XVIIIE1 T5I2 R23 C9 r3-c2 r4-c4 unguiculata}PIR|T08124|T08124 ferritin 2 precursor- cowp tomato invertase inhibitor TC76975 AI782237 cLES18F9 XF8 T3K16 R9 C11 r2-c1 r4-c3 chalcone--flavanone isomerase a {Petunia TC76987 BG126620 cTOF12L6 XVIIIH8 T5O16 R9 C15 r3-c2 r4-c4 hybrida}SP|P11650|CFIA_PETHY CHALCONE-- FLAVONONE ISOMERASE 3-ketoacyl-CoA thiolase {Arabidopsis TC76988 AI775821 cLER16N17 VC4 T2E7 R18 C5 r4-c2 r1-c3 thaliana}GP|2981618|dbj|BAA25249.1||AB008855 3- ketoacyl-CoA th chalcone synthase TC77000 BE435825 cLEG29O5 VH12 T2O23 R2 C15 r4-c2 r1-c3 contains similarity to diaminopimelate TC77005 AW928611 cTOC2D23 XVIID3 T5G5 R20 C7 r3-c2 r4-c4 decarboxylase~gene_id: MLN21.17 {Arabidopsis thaliana} glyceraldehyde 3-phosphate dehydrogenase TC77013 AW647921 cLEI2J10 VIID6 T2H11 R14 C8 r4-c2 r1-c3 aspartate aminotransferase {Medicago TC77015 BG127416 cTOF16M22 XVIID6 T5G11 R14 C7 r3-c2 r4-c4 sativa}□GP|777387|gb|AAB46611.1||L25335 aspartate aminotransfer Contains similarity to a putative 6- TC77016 AW219887 cLEX6G21 XIIIE11 T4I21 R4 C9 r2-c2 r1-c4 phosphogluconolactonase T1G12.6 GP|6553917 from Arabidopsis thal WRKY transcription factor Nt-SubD48 {Nicotiana TC77024 AW034258 cLEC38A11 XVIG11 T4N22 R3 C14 r2-c2 r1-c4 tabacum} glutamate decarboxylase isozyme 4 {Nicotiana TC77052 AW030295 cLEC18C17 ID11 T1G21 R4 C7 r1-c2 r3-c3 tabacum} D-3-PHOSPHOGLYCERATE DEHYDROGENASE TC77066 BE451433 cLEY18P1 XIVA11 T4A22 R3 C1 r2-c2 r1-c4 PRECURSOR (EC 1.1.1.95) (PGDH).GP|2189964|dbj|BAA20405.1||AB0032 putative glucosyl transferase {Arabidopsis TC77071 AW737341 cTOD3O15 VIE2 T2I4 R21 C9 r4-c2 r1-c3 thaliana}PIR|H84784|H84784 probable glucosyl transferase 11S globulin precursor {Sesamum indicum} TC77083 BF051303 cLEM22M13 IVD3 T1H6 R19 C8 r1-c2 r3-c3 Putative ABC transporter {Arabidopsis TC77089 AI490083 cLED19M7 IIIB11 T1D21 R4 C4 r1-c2 r3-c3 thaliana}PIR|H96622|H96622 probable ABC transporter F23H11.19 putative fatty acid desaturase {Arabidopsis TC77096 AW038672 cLET2D1 XIG10 T3N19 R6 C14 r2-c1 r4-c3 thaliana}GP|4325341|gb|AAD17340.1||AF128393 similar to S-adenosyl-L-methionine:salicylic acid carboxyl TC77118 BE459581 cLEM7O9 VIIIF1 T2L2 R23 C12 r4-c2 r1-c3 methyltransferase {Stephanotis floribunda} putative hydroxymethylglutaryl-CoA lyase protein TC77127 AW217746 cTOC6G1 XVIIE6 T5I11 R14 C9 r3-c2 r4-c4 {Arabidopsis thaliana}GP|13194812|gb|AAK15568.1|AF PYRROLINE-5-CARBOXYLATE REDUCTASE (EC TC77132 BF051120 cLEM21L1 VIIIA6 T2B12 R13 C2 r4-c2 r1-c3 1.5.1.2) (P5CR) (P5C REDUCTASE).GP|1928962|gb|AAC14482.1||U92 putative transcription factor {Oryza TC77133 AW944929 cTOB12J3 XVIG10 T4N20 R5 C14 r2-c2 r1-c4 sativa}GP|12328532|dbj|BAB21190.1||AP002909 putative transcrip S-adenosylmethionine:2-demethylmenaquinone TC77161 BG127962 cTOF18H11 XIXB11 T5D21 R4 C4 r3-c2 r4-c4 methyltransferase-like {Arabidopsis thaliana} UDP rhamnose: anthocyanidin-3-glucoside TC77166 BE432345 cLEG7H11 VIH7 T2O14 R11 C15 r4-c2 r1-c3 rhamnosyltransferase {Petunia x hybrida}PIR|S36655|S36655 U phosphoenolpyruvate carboxylase kinase TC77168 BE431605 cLEG27M9 VH3 T2O5 R20 C15 r4-c2 r1-c3 putative aspartate aminotransferase {Arabidopsis TC77175 BG123217 cTOF1O17 XIXD9 T5H17 R8 C8 r3-c2 r4-c4 thaliana}PIR|E84610|E84610 probable aspartate amin ADP-glucose pyrophosphorylase large subunit TC77179 BE459469 cLEM6L16 VIIIE5 T2J10 R15 C10 r4-c2 r1-c3 threonine synthase {Solanum tuberosum} TC77196 AW091608 cLET15L20 XID5 T3H9 R16 C8 r2-c1 r4-c3 tryptophan synthase beta chain {Arabidopsis thaliana} TC77225 BF051762 cLEM24I23 VIIIC6 T2F12 R13 C6 r4-c2 r1-c3 putative C3HC4-type RING zinc finger/ankyrin protein TC77229 AW929405 cTOC8B24 IVG12 T1N24 R1 C14 r1-c2 r3-c3 {Arabidopsis thaliana}PIR|E84689|E84689 probab UMP/CMP kinase like protein {Arabidopsis TC77240 BF050903 cLEM19L18 VIIH7 T2P13 R12 C16 r4-c2 r1-c3 thaliana}GP|7269379|emb|CAB81339.1||AL161563 UMP/CMP kinas PROBABLE UDP-GLUCOSE 4-EPIMERASE TC77242 AW738215 cTOD5J9 XVIIH9 T5O17 R8 C15 r3-c2 r4-c4 AT4G23920 (EC 5.1.3.2) (GALACTOWALDENASE) (UDP-GALACTOSE 4-EPIMERAS putative zinc finger protein {Oryza sativa} TC77251 AW737484 cTOD3I18 XVIIG9 T5M17 R8 C13 r3-c2 r4-c4 fructose-1,6-biphosphatase TC77264 BG131255 cTOE3E20 XVIIIF5 T5K10 R15 C11 r3-c2 r4-c4 shikimate kinase precursor TC77265 AI773666 cLER7F8 IVH5 T1P10 R15 C16 r1-c2 r3-c3 shikimate kinase precursor {Lycopersicon TC77266 BE433355 cLEG13C20 VE3 T2I5 R20 C9 r4-c2 r1-c3 esculentum}SP|Q00497|AROK_LYCES SHIKIMATE KINASE PRECURSOR putative sugar transporter TC77279 AI489511 cLED16M9 IIIA10 T1B19 R6 C2 r1-c2 r3-c3 S-adenosyl-L-methionine:salicylic acid carboxyl TC77297 AW929283 cTOC7K17 XVIIE10 T5I19 R6 C9 r3-c2 r4-c4 methyltransferase {Atropa belladonna} G-box binding protein TC77305 AI487557 cLED9N21 IVD2 T1H4 R21 C8 r1-c2 r3-c3 unnamed protein product TC77310 BE460937 cLEG37A9 VID5 T2G10 R15 C7 r4-c2 r1-c3 {unidentified}GP|6683619|dbj|BAA89269.1||AB025250 ATP phosphoribosyl transf putative NADH dehydrogenase (ubiquinone TC77318 BG643872 cTOF33I9 XXD2 T5H4 R21 C8 r3-c2 r4-c4 oxidoreductase) {Arabidopsis thaliana}PIR|T02486|T02486 hyp contains similarity to transcription TC77334 AI896178 cLEC14E22 IB12 T1C23 R2 C3 r1-c2 r3-c3 regulator~gene_id: MRG7-19 {Arabidopsis thaliana} G-box binding protein TC77337 BG129706 cTOF27L18 XXA5 T5B10 R15 C2 r3-c2 r4-c4 NADH dehydrogenase {Solanum TC77343 BG128821 cTOF22M16 XIXF2 T5L3 R22 C12 r3-c2 r4-c4 tuberosum}SP|P80269|NUIM_SOLTU NADH- UBIQUINONE OXIDOREDUCTASE 23 KDA SU phosphatidylserine decarboxylase {Arabidopsis TC77346 BE434333 cLEG16I23 VF1 T2K1 R24 C11 r4-c2 r1-c3 thaliana} PHLH transcription factor JAF13 {Petunia x hybrida} TC77374 AI489467 cLED16J1 IIH4 T1O8 R17 C15 r1-c2 r3-c3 nitrite reductase {Capsicum annuum} TC77375 BF098124 cLEW25H15 XIIG9 T3N18 R7 C14 r2-c1 r4-c3 putative aminotransferase; 101422-99564 {Arabidopsis TC77383 AI777500 cLES1L18 XXIC1 T6E1 R24 C5 r3-c1 r2-c4 thaliana}PIR|D96806|D96806 probable aminotrans VACUOLAR ATP SYNTHASE 16 KDA TC77384 AW092235 cLET18D11 XID11 T3H21 R4 C8 r2-c1 r4-c3 PROTEOLIPID SUBUNIT (EC 3.6.1.34) (V-ATPASE 16 KDA PROTEOLIPID SUBUNIT cytochrome c oxidase subunit Vb precursor-like protein TC77386 BE436938 cLEG34P1 VIC4 T2E8 R17 C5 r4-c2 r1-c3 {Arabidopsis thaliana} PROBABLE RIBOSE 5-PHOSPHATE ISOMERASE TC77390 AI775880 cLER16H24 IXG6 T3M11 R14 C13 r2-c1 r4-c3 (EC 5.3.1.6) (PHOSPHORIBOISOMERASE).GP|4262236|gb|AAD14529.1| phosphoenolpyruvate carboxylase 1 TC77403 AI781606 cLES16D23 IVF4 T1L8 R17 C12 r1-c2 r3-c3 nitrite reductase {Capsicum annuum} TC77408 BF113958 cLEY23O22 XIVC1 T4E2 R23 C5 r2-c2 r1-c4 hypothetical protein {Arabidopsis TC77438 BG130561 cTOF31B5 XXC2 T5F4 R21 C6 r3-c2 r4-c4 thaliana}GP|3281856|emb|CAA19751.1||AL031004 Transcription factor putative glucose-6-phosphate/phosphate-tranlocat or TC77448 AI895217 cLEC7I15 IIF1 T1K2 R23 C11 r1-c2 r3-c3 {Oryza sativa} uroporphyrinogen decarboxylase precursor {Nicotiana TC77455 AI778274 cLES4D24 XVID2 T4H4 R21 C8 r2-c2 r1-c4 tabacum}SP|Q42967|DCUP_TOBAC UROPORPHYRINOGEN D putative strictosidine synthase; 35901-37889 TC77457 BE449584 cLHT32E19 XVC7 T4F13 R12 C6 r2-c2 r1-c4 {Arabidopsis thaliana}PIR|A96768|A96768 protein strict putative aminotransferase {Arabidopsis thaliana} TC77480 AI489286 cLED17E18 IIIA12 T1B23 R2 C2 r1-c2 r3-c3 TRANSCRIPTION INITIATION FACTOR TFIID 100 KDA TC77486 BE432492 cLEG8016 VIIA2 T2B3 R22 C2 r4-c2 r1-c3 SUBUNIT (TAFII-100) (TAFII100).GP|1932938|gb|AAC51215 putative glucosyl transferase {Arabidopsis TC77491 AI485737 cLED4G20 IVA5 T1B10 R15 C2 r1-c2 r3-c3 thaliana}PIR|C84784|C84784 probable glucosyl transferase glucose-6-phosphate 1-dehydrogenase {Solanum TC77502 BE459880 cLEM8E24 IVG2 T1N4 R21 C14 r1-c2 r3-c3 tuberosum}SP|P37830|G6PD_SOLTU GLUCOSE-6- PHOSPHATE 1-D omega-6 fatty acid desaturase {Sesamum indicum} TC77526 AW031750 cLEC21B10 IE8 T1I15 R12 C9 r1-c2 r3-c3 putative C3HC4-type RING zinc finger protein TC77528 AW738118 cTOD5E12 XVIIH8 T5O15 R12 C15 r3-c2 r4-c4 {Arabidopsis thaliana}PIR|T02413|T02413 probable RING Alfin-1 {Medicago sativa}PIR|T09646|T09646 probable TC77531 BG643537 cTOF31G7 XXC5 T5F10 R15 C6 r3-c2 r4-c4 zinc finger protein-alfalfa (fragment) putative ABC transporter; 66585-65723 {Arabidopsis TC77538 AI775901 cLER16L22 IXG9 T3M17 R8 C13 r2-c1 r4-c3 thaliana}PIR|C96702|C96702 probable ABC transpor phosphoribosyl pyrophosphate synthase isozyme 3 TC77539 AI781720 cLES16L10 XE12 T3I24 R1 C9 r2-c1 r4-c3 {Spinacia oleracea} TRYPTOPHAN SYNTHASE BETA CHAIN 2 TC77555 AI488512 cLED23N20 IIIC10 T1F19 R6 C6 r1-c2 r3-c3 PRECURSOR (EC 4.2.1.20).GP|2792520|gb|AAB97087.1||AF042320 tryptop indole-3-glycerol phosphate synthase {Arabidopsis TC77561 AW618611 cLPT14I1 XVG7 T4N13 R12 C14 r2-c2 r1-c4 thaliana} cytochrome P450 {Solanum tuberosum} TC77562 AI896104 cLEC13J4 IC11 T1E21 R4 C5 r1-c2 r3-c3 acetyl-CoA carboxylase {Medicago TC77572 BE433724 cLEG20L23 VG4 T2M7 R18 C13 r4-c2 r1-c3 sativa}GP|495725|gb|AAB42144.1||L25042 acetyl-CoA carboxylase {Med 3-isopropylmalate dehydratase, small subunit TC77576 AW649879 cLEI9P8 VIIG8 T2N15 R12 C14 r4-c2 r1-c3 {Arabidopsis thaliana}PIR|H84861|H84861 3- isopropylmal MADS-box transcription factor FBP22 {Petunia x TC77597 AW623098 cTOB8E22 XVIIB9 T5C17 R8 C3 r3-c2 r4-c4 hybrida} probable UDP-glucuronosyltransferase (EC 2.4.1.—)- TC77599 AI897234 cLED27K11 IIIE2 T1J3 R22 C10 r1-c2 r3-c3 garden pea NADH dehydrogenase {Solanum TC77602 AW929834 cTOC5H20 XVIIE2 T5I3 R22 C9 r3-c2 r4-c4 tuberosum}GP|639834|emb|CAA58823.1||X83999 NADH dehydrogenase {Solanum phosphoglucomutase-like protein {Arabidopsis TC77603 BG135437 cTOE22H5 XVIIIE5 T5I10 R15 C9 r3-c2 r4-c4 thaliana}PIR|T51457|T51457 phosphoglucomutase-like pro biotin-binding protein{circumflex over ( )}{circumflex over ( )}biotin-containing subunit of TC77606 BF112416 cLEG41E6 VIF2 T2K4 R21 C11 r4-c2 r1-c3 methylcrotonyl-CoA carboxylase ATP:citrate lyase {Capsicum annuum} TC77626 AW617219 cLHT22E7 XIIIB12 T4C23 R2 C3 r2-c2 r1-c4 putative cytochrome P450 {Solanum TC77648 AI771126 cLED28H13 IIIE3 T1J5 R20 C10 r1-c2 r3-c3 chacoense}SP|P93530|C7D6_SOLCH CYTOCHROME P450 71D6 (EC 1.14.—.—) cytochrome c oxidase subunit 6b {Oryza TC77660 AI484719 cLED3L3 IVA2 T1B4 R21 C2 r1-c2 r3-c3 sativa}GP|9967162|dbj|BAB12275.1||AB047923 cytochrome c oxid glycerol-3-phosphate acyltransferase {Cucumis TC77666 AW623199 cTOB9G15 XVIIB12 T5C23 R2 C3 r3-c2 r4-c4 sativus}SP|Q39639|PLSB_CUCSA GLYCEROL-3- PHOSPHATE ACY S-adenosyl-L-methionine:salicylic acid carboxyl TC77684 AW738171 cTOD5O22 XVIIIB5 T5C10 R15 C3 r3-c2 r4-c4 methyltransferase-like protein {Arabidopsis thaliana 3-deoxy-D-arabino-heptulosonate 7-phosphate synthase TC77693 AW738296 cTOD6J18 XVIIIA3 T5A6 R19 C1 r3-c2 r4-c4 {Morinda citrifolia} serine hydroxymethyltransferase, mitochondrial TC77724 BE460801 cLEG36D13 VIC10 T2E20 R5 C5 r4-c2 r1-c3 precursor (serine methylase) (glycine hydroxymethyltr putative sugar transporter {Arabidopsis thaliana} TC77728 AW622974 cTOB7H5 IVG4 T1N8 R17 C14 r1-c2 r3-c3 alpha-glucan phosphorylase, 1 isozyme 2 precursor TC77734 AW738276 cTOD6F22 IA1 T1A1 R24 C1 r1-c2 r3-c3 (starch phosphorylase 1-2) {Solanum tuberosum}SP| HB2 homeodomain protein {Populus tremula x Populus TC77747 AW618062 cLPT11L16 XVF11 T4L21 R4 C12 r2-c2 r1-c4 tremuloides} Strong similarity to gb|U61231 cytochrome P450 from TC77757 AI484951 cLED2F4 IIIE9 T1J17 R8 C10 r1-c2 r3-c3 Arabidopsis thaliana and is a member of the PF|0 succinyl-CoA synthetase, alpha subunit {Arabidopsis TC77763 BG125244 cTOF8E15 XVIF9 T4L18 R7 C12 r2-c2 r1-c4 thaliana} NADH dehydrogenase {Solanum TC77792 AI778324 cLES4P12 XH9 T3O18 R7 C15 r2-c1 r4-c3 tuberosum}GP|639834|emb|CAA58823.1||X83999 NADH dehydrogenase {Solanum glucose-6-phosphate/phosphate-translocator precursor TC77793 BE450870 cLEY15O8 XIIIH9 T4O17 R8 C15 r2-c2 r1-c4 {Pisum sativum}PIR|T06254|T06254 glucose-6-pho pyrophosphate-fructose 6-phosphate 1- TC77808 BE434021 cLEG13H5 XVIH1 T4P2 R23 C16 r2-c2 r1-c4 phosphotransferase alpha subunit (pfp) (6- phosphofructokinase adenosine kinase {Arabidopsis TC77810 AW615848 cTOA17I8 XVID10 T4H20 R5 C8 r2-c2 r1-c4 thaliana}GP|7378610|emb|CAB83286.1||AL162751 adenosine kinase-like pr sucrose transporter {Lycopersicon esculentum} TC77814 BF050231 cLEM17E17 VIIG10 T2N19 R6 C14 r4-c2 r1-c3 transketolase 1 {Capsicum TC77838 AW442085 cLEN21E6 IXB12 T3C23 R2 C3 r2-c1 r4-c3 annuum}PIR|T09541|T09541 transketolase (EC 2.2.1.1) TKT1 precursor, chlor transcription factor inhibitor I kappa B homolog TC77842 BE432768 cLEG10A24 VH2 T2O3 R22 C15 r4-c2 r1-c3 {Arabidopsis thaliana}GP|1773295|gb|AAC49611.1||U7 aspartate-semialdehyde dehydrogenase precursor TC77844 BG124618 cTOF5F3 XXH3 T5P6 R19 C16 r3-c2 r4-c4 {Arabidopsis thaliana} putative flavonol 3-O-glucosyltransferase {Arabidopsis TC77847 AW091930 cLET17G11 VIIF1 T2L1 R24 C12 r4-c2 r1-c3 thaliana}PIR|F84618|F84618 probable flavonol ornithine carbamoyltransferase; OCTase {Canavalia TC77862 BG130753 cTOE1M7 XVIIID11 T5G22 R3 C7 r3-c2 r4-c4 lineata}GP|12003188|gb|AAG43481.1|AF203688_1|AF20 NADH-dependent glutamate synthase {Medicago TC77867 BE449812 cLEY14O21 XIIIG12 T4M23 R2 C13 r2-c2 r1-c4 sativa} contains similarity to transcription TC77873 BE436142 cLEG30J20 VIA3 T2A6 R19 C1 r4-c2 r1-c3 regulator~gene_id: MRG7.19 {Arabidopsis thaliana} contains similarity to C2H2-type zinc finger TC77881 AW648552 cLEI4P14 VC8 T2E15 R12 C5 r4-c2 r1-c3 protein~gene_id: MOK16.6 {Arabidopsis thaliana} putative zinc finger protein {Oryza sativa} TC77907 AW094020 cLET27A3 XVIIE9 T5I17 R8 C9 r3-c2 r4-c4 putative hydroxymethyltransferase; 49598-47322 TC77914 AW030791 cLEC22A6 XXIIA2 T6A4 R21 C1 r3-c1 r2-c4 {Arabidopsis thaliana}PIR|F86484|F86484 probable hyd deoxyuridine triphosphatase, dUTPase, P18 {EC TC77923 AI486505 cLED6E4 IVB7 T1D14 R11 C4 r1-c2 r3-c3 3.6.1.23} [tomatoes, Tint Tim cultivar LA154, Peptide, 169 aa] cytochome P450, putative {Arabidopsis TC77959 AI773114 cLER5K20 XC1 T3E2 R23 C5 r2-c1 r4-c3 thaliana}PIR|F86441|F86441 probable cytochrome P450 [importe NAD-malate dehydrogenase {Nicotiana tabacum} TC77971 BE435129 cLEG25M1 XVIIC12 T5E23 R2 C5 r3-c2 r4-c4 aspartate aminotransferase {Panicum TC77973 AI898706 cLED35I22 IIIG11 T1N21 R4 C14 r1-c2 r3-c3 miliaceum}GP|20597|emb|CAA45022.1||X63428 aspartate aminotransf phosphoenolpyruvate carboxylase {Nicotiana TC77975 BF114018 cLEY23H10 XIVB12 T4C24 R1 C3 r2-c2 r1-c4 tabacum}SP|P27154|CAPP_TOBAC PHOSPHOENOLPYRUVATE CARBOXY Contains similarity to DNA-binding protein MYB1 TC77983 BE450376 cLEY13G13 XIIIG2 T4M3 R22 C13 r2-c2 r1-c4 from Petroselinum crispum GP|7488946 and contains MY phosphatidylinositol 4-kinase {Solanum tuberosum} TC78010 AI771897 cLED38E12 IIIH5 T1P9 R16 C16 r1-c2 r3-c3 L-allo-threonine aldolase homolog F22O13.11- TC78023 BE437087 cLEG35M18 XIF12 T3L23 R2 C12 r2-c1 r4-c3 Arabidopsis thaliana argininosuccinate synthase-like protein {Arabidopsis TC78033 AW029695 cLEC11G5 IC2 T1E3 R22 C5 r1-c2 r3-c3 thaliana}GP|7269334|emb|CAB79393.1||AL161562 a hyoscyamine 6-dioxygenase hydroxylase, putative TC78043 BE434473 cLEG17M15 VF6 T2K11 R14 C11 r4-c2 r1-c3 {Arabidopsis thaliana}PIR|G86472|G86472 probable hy SNF2 subfamily global transcription activator. TC78051 BG127884 cTOF18K14 XIXC1 T5F1 R24 C6 r3-c2 r4-c4 {Arabidopsis thaliana}PIR|G84897|G84897 hypothetical CYTOCHROME P450 98A2 (EC 1.14.—.—). TC78082 AI895234 cLEC7M3 IIF3 T1K6 R19 C11 r1-c2 r3-c3 GP|2738998|gb|AAB94587.1||AF022458 CYP98A2p {Glycine max}PIR|T0 branched-chain amino acid aminotransferase {Solanum TC78133 AW034526 cLEC24K18 IF7 T1K13 R12 C11 r1-c2 r3-c3 tuberosum} geranylgeranyl pyrophosphate synthase-related protein TC78147 BE436393 cLEG32A20 XIH4 T3P7 R18 C16 r2-c1 r4-c3 {Arabidopsis thaliana}GP|7270829|emb|CAB80510 putative phosphatidylserine decarboxylase {Arabidopsis TC78160 BF112654 cLEG42C5 VIF7 T2K14 R11 C11 r4-c2 r1-c3 thaliana}GP|7269448|emb|CAB79452.1||AL161564 cytochrome P450 {Catharanthus TC78161 AW035889 cLEC35F7 IIB3 T1C6 R19 C3 r1-c2 r3-c3 roseus}PIR|T09999|T09999 cytochrome P450- Madagascar periwinkle CYTOCHROME P450 71A9 (EC 1.14.—.—) (P450 TC78170 AW031676 cLEC37B20 IIB12 T1C24 R1 C3 r1-c2 r3-c3 CP1).GP|3334659|emb|CAA71513.1||Y10489 putative cytochrome bA554C12.1 (RBX1 or ROC1 (ring-box or ring finger TC78191 AW092264 cLET18J1 XID12 T3H23 R2 C8 r2-c1 r4-c3 protein 1)) {Homo sapiens}GP|4769004|gb|AAD29715. alpha amylase precursor {Cuscuta TC78197 BE460877 cLEG36F6 VIC11 T2E22 R3 C5 r4-c2 r1-c3 reflexa}GP|458456|gb|AAA16513.1||U06754 alpha amylase precursor {C putative strictosidine synthase-like {Arabidopsis TC78210 BG628308 cLEL21K15 XXIE5 T6I9 R16 C9 r3-c1 r2-c4 thaliana} malate dehydrogenase, mitochondrial precursor TC78217 BG134615 cTOE16N4 XVIIID2 T5G4 R21 C7 r3-c2 r4-c4 {Citrullus vulgaris}EGAD|148462|158380 hypothetical p flavanone 3-hydroxylase {Citrus sinensis} TC78218 BG628122 cLEL20G15 XXIE3 T6I5 R20 C9 r3-c1 r2-c4 Contains similarity to gb|Y13720 Hap2a transcription TC78236 BF051108 cLEM21H2 VIIIA5 T2B10 R15 C2 r4-c2 r1-c3 factor from Arabidopsis thaliana.PIR|A86430|A8 GALACTOKINASE (EC 2.7.1.6) (GALACTOSE TC78245 AW624648 cTOB16F12 XVIIA6 T5A11 R14 C1 r3-c2 r4-c4 KINASE).GP|12322687|gb|AAG51339.1|AC020580_19 AC020580 galact DIACYLGLYCEROL KINASE 1 (EC 2.7.1.107) TC78269 AI486282 cLED8G16 IVC8 T1F16 R9 C6 r1-c2 r3-c3 (DIGLYCERIDE KINASE) (DGK 1) (DAG KINASE 1).GP|1374772|dbj|B myb-related transcription factor LBM1 {Nicotiana TC78270 AW030476 cLEC11D10 IIB5 T1C10 R15 C3 r1-c2 r3-c3 tabacum} transcription factor {Vicia TC78324 BG126414 cTOF12A24 XVIIIH1 T5O2 R23 C15 r3-c2 r4-c4 faba}GP|2104679|emb|CAA66480.1||X97906 transcription factor {Vicia faba alpha-glucan phosphorylase, h isozyme phosphorylase TC78327 AW616770 cLHT12L6 XVA2 T4B3 R22 C2 r2-c2 r1-c4 h) {Solanum tuberosum}SP|P32811|PHSH_SOLTU ALPH isocitrate dehydrogenase (NAD+) {Solanum TC78346 BG644139 cTOF34O17 XXD7 T5H14 R11 C8 r3-c2 r4-c4 tuberosum} NADH dehydrogenase (ubiquinone) (EC 1.6.5.3) chain TC78368 AI485504 cLED7A14 IVC3 T1F6 R19 C6 r1-c2 r3-c3 nad9-wheat mitochondrion Zn finger protein {Nicotiana TC78369 BF097661 cLEW23I9 XIIG5 T3N10 R15 C14 r2-c1 r4-c3 tabacum}GP|1360086|emb|CAA66605.1||X97946 Zn finger protein {Nicotiana flavonoid 3′,5′-hydroxylase-like; cytochrome P450 TC78380 AW623747 cTOB13C13 XVIG5 T4N10 R15 C14 r2-c2 r1-c4 {Arabidopsis thaliana} geranylgeranyl pyrophosphate synthetase precursor TC78381 BE434535 cLEG17J7 VIIA7 T2B13 R12 C2 r4-c2 r1-c3 (ggpp synthetase) (dimethylallyltransferase {Capsi MYB-like DNA-binding domain protein {Gossypium TC78385 AI488744 cLED13H15 IIH6 T1O12 R13 C15 r1-c2 r3-c3 hirsutum}PIR|T09745|T09745 myb-related protein-upl homeobox 2 protein TC78390 AI897002 cLED26E23 IIID9 T1H17 R8 C8 r1-c2 r3-c3 Contains similarity to dTPD-D-glucose-4,6-dehydratase TC78391 AI486284 cLED8I4 IVC9 T1F18 R7 C6 r1-c2 r3-c3 from Sphingomonas sp.S88 gb|U51197 and contain fructokinase TC78393 BF098243 cLEW26O6 XIIH2 T3P4 R21 C16 r2-c1 r4-c3 fructose-6-phosphate 2-kinase/fructose-2,6- TC78403 AI896831 cLEC23B12 IF1 T1K1 R24 C11 r1-c2 r3-c3 bisphosphatase {Solanum tuberosum}PIR|T07016|T07016 6-ph cytochrome P450 {Nicotiana TC78431 AW616606 cLHT11J2 XIVH9 T4O18 R7 C15 r2-c2 r1-c4 tabacum}GP|1171579|emb|CAA64635.1||X95342 cytochrome P450 {Nicotiana tab MADS-box transcription factor FBP21 {Petunia x TC78439 AW039132 cLET8H21 XIIC9 T3F18 R7 C6 r2-c1 r4-c3 hybrida} 76 kDa mitochondrial complex I subunit {Solanum TC78448 BE460354 cLEG28D24 VH5 T2O9 R16 C15 r4-c2 r1-c3 tuberosum}SP|Q43644|NUAM_SOLTU NADH- UBIQUINONE OXID contains similarity to SNF2/RAD54 family (RAD26 TC78453 AW615869 cTOA17M20 XVIE2 T4J4 R21 C10 r2-c2 r1-c4 subfamily) transcription-repair coupling factor~gene homeodomain protein {Malus x domestica} TC78458 AW031305 cLEC35K11 IIB7 T1C14 R11 C3 r1-c2 r3-c3 transcription regulator Sir2-like protein {Arabidopsis TC78492 AW441312 cLEN15I15 IXA5 T3A9 R16 C1 r2-c1 r4-c3 thaliana}GP|12006420|gb|AAG44850.1|AF283757_(—) pyrophosphate-dependent phosphofructokinase beta TC78498 AI896796 cLEC23J17 IF2 T1K3 R22 C11 r1-c2 r3-c3 subunit {Citrus x paradisi} CYP83D1p {Glycine max}PIR|T05940|T05940 TC78508 BG125130 cTOF7B4 XXF5 T5L10 R15 C12 r3-c2 r4-c4 cytochrome P450 83D1p-soybean (fragment) Putative UDP-glucose:sterol glucosyltransferase TC78531 BG128011 cTOF18B24 XIXB8 T5D15 R12 C4 r3-c2 r4-c4 {Arabidopsis thaliana}PIR|D96499|D96499 probable UD contains similarity to cyclopropane fatty acid TC78544 AW399730 cLPT8J6 XVIC4 T4F8 R17 C6 r2-c2 r1-c4 synthase~gene_id: MEE5.5 {Arabidopsis thaliana} zinc finger and C2 domain protein {Arabidopsis TC78550 AW039744 cLET13K10 XIC11 T3F21 R4 C6 r2-c1 r4-c3 thaliana} cinnamoyl CoA reductase-like protein {Arabidopsis TC78570 BE433500 cLEG15E22 VE7 T2I13 R12 C9 r4-c2 r1-c3 thaliana}PIR|T48643|T48643 cinnamoyl CoA reductas tyrosine aminotransferase-like protein {Arabidopsis TC78598 BF096944 cLEW18G10 XIIE1 T3J2 R23 C10 r2-c1 r4-c3 thaliana} omega-3 fatty acid desaturase, endoplasmic reticulum TC78627 BG629236 cLEL2K2 XXIG3 T6M5 R20 C13 r3-c1 r2-c4 {Nicotiana tabacum}SP|P48626|FD3E_TOBAC OMEGA- anthranilate phosphoribosyltransferase-like protein TC78632 AW650876 cLEI14P19 VIIC4 T2F7 R18 C6 r4-c2 r1-c3 {Arabidopsis thaliana}PIR|T46010|T46010 anthran putative folylpolyglutamate synthetase {Oryza sativa} TC78676 BE441141 cLEM6E13 VIIIE2 T2J4 R21 C10 r4-c2 r1-c3 transcription factor IIA large subunit {Arabidopsis TC78698 AI894579 cLEC4L15 IID10 T1G20 R5 C7 r1-c2 r3-c3 thaliana}PIR|T51333|T51333 transcription factor putative alpha-amylase; 60344-64829 {Arabidopsis TC78700 BE436615 cLEG33F11 VIB9 T2C18 R7 C3 r4-c2 r1-c3 thaliana}PIR|E96720|E96720 probable alpha-amylase polyneuridine aldehyde esterase {Rauvolfia serpentina} TC78712 BG126704 cTOF13K13 XVIIIH9 T5O18 R7 C15 r3-c2 r4-c4 2S seed albumin-1 large subunit [Lycopersicon TC78715 AW036308 cLEE1G12 IVD5 T1H10 R15 C8 r1-c2 r3-c3 esculentum] Strong similarity to F19I3.8 GP|3033381 putative UDP- TC78747 AW623155 cTOB8J19 XVIIB11 T5C21 R4 C3 r3-c2 r4-c4 galactose-4-epimerase from Arabidopsis thaliana Similar to gb|AF135422 GDP-mannose TC78749 AW094226 cLET27N17 XXID12 T6G23 R2 C7 r3-c1 r2-c4 pyrophosphorylase A (GMPPA) from Homo sapiens. ESTs gb|AA712990, heat stress transcription factor 8 TC78884 AW223123 cLEN10H3 VIIIG3 T2N6 R19 C14 r4-c2 r1-c3 pyruvate kinase, cytosolic isozyme {Nicotiana TC78918 AI897691 cLED30K3 IIIF6 T1L11 R14 C12 r1-c2 r3-c3 tabacum}SP|Q42954|KPYC_TOBAC PYRUVATE KINASE, CYTOSOL 2-oxoglutarate/malate translocator precursor-like protein TC78921 BG125571 cTOF9G3 XVIIH6 T5O11 R14 C15 r3-c2 r4-c4 {Arabidopsis thaliana}PIR|T49900|T49900 2 cytochrome P450 {Solanum tuberosum} TC78950 BG131258 cTOE3G12 XVIIIF6 T5K12 R13 C11 r3-c2 r4-c4 CYTOCHROME P450 97B2 (EC 1.14.—.—). TC78953 AI482691 cLEB1L15 IA7 T1A13 R12 C1 r1-c2 r3-c3 GP|2738996|gb|AAB94586.1||AF022457 CYP97B2p {Glycine max}PIR|T0 alpha-glucosidase {Solanum TC78967 BE435693 cLEG28I14 VH7 T2O13 R12 C15 r4-c2 r1-c3 tuberosum}PIR|T07391|T07391 probable alpha- glucosidase (EC 3.2.1.20)-p threonine synthase {Solanum tuberosum} TC78978 AW092379 cLET20E24 XIE10 T3J19 R6 C10 r2-c1 r4-c3 NADH dehydrogenase subunit TC79000 AI775474 cLER15L15 IXF11 T3K21 R4 C11 r2-c1 r4-c3 RING-H2 finger protein RHF2a {Arabidopsis TC79012 BG134178 cTOE15F13 VIIIC8 T2F16 R9 C6 r4-c2 r1-c3 thaliana}GP|13374859|emb|CAC34493.1||AL589883 RING-H2 fin putative C3HC4-type RING zinc finger/ankyrin protein TC79013 AI483217 cLEB8I19 IIB8 T1C16 R9 C3 r1-c2 r3-c3 {Arabidopsis thaliana}PIR|E84689|E84689 probab Dof zinc finger protein {Solanum tuberosum} TC79103 AW622638 cLEX15J2 XIIIC12 T4E23 R2 C5 r2-c2 r1-c4 glucose acyltransferase {Lycopersicon pennellii} TC79131 AW399149 cLPT6K12 XVIB11 T4D22 R3 C4 r2-c2 r1-c4 tyrosine decarboxylase {Arabidopsis thaliana} TC79134 AW217489 cTOB1E23 XVIIA10 T5A19 R6 C1 r3-c2 r4-c4 aldose-1-epimerase-like protein {Nicotiana TC79135 BE450681 cLEY14N1 XIIIG9 T4M17 R8 C13 r2-c2 r1-c4 tabacum}PIR|T01933|T01933 probable aldose 1- epimerase (E putative ABC transporter {Arabidopsis TC79147 AW932006 cLEF47A5 IVH3 T1P6 R19 C16 r1-c2 r3-c3 thaliana}GP|4115931|gb|AAD03441.1||AF118223 contains similari polyneuridine aldehyde esterase {Rauvolfia serpentina} TC79199 AW621893 cLEX13L15 XIIIC5 T4E9 R16 C5 r2-c2 r1-c4 glycogen (starch) synthase precursor {Solanum TC79234 AW399814 cLPT10L12 XVF9 T4L17 R8 C12 r2-c2 r1-c4 tuberosum}SP|Q00775|UGST_SOLTU GRANULE- BOUND GLYCOGEN alpha glucosidase-like protein {Arabidopsis thaliana} TC79238 AW223788 cLEN13L15 VIIIH7 T2P14 R11 C16 r4-c2 r1-c3 transcription factor TEIL {Nicotiana tabacum} TC79239 BF112869 cLEG42L9 VIF9 T2K18 R7 C11 r4-c2 r1-c3 neutral invertase, putative {Arabidopsis TC79243 BG129477 cTOF24J3 XIXG7 T5N13 R12 C14 r3-c2 r4-c4 thaliana}GP|12324537|gb|AAG52223.1|AC021665_6|AC021665 put putative alpha-amylase; 60344-64829 {Arabidopsis TC79253 BE461271 cLEG38E23 VIE1 T2I2 R23 C9 r4-c2 r1-c3 thaliana}PIR|E96720|E96720 probable alpha-amylase HOMEOBOX-LEUCINE ZIPPER PROTEIN HAT7 TC79277 BF098451 cLEW27E6 XIIH4 T3P8 R17 C16 r2-c1 r4-c3 (HD-ZIP PROTEIN 7) (HD-ZIP PROTEIN ATHB- 3).GP|549891|gb|AAA569 Similar to UTP-glucose glucosyltransferases TC79292 AI779058 cLES7A11 XIA6 T3B11 R14 C2 r2-c1 r4-c3 {Arabidopsis thaliana}PIR|G86144|G86144 hypothetical pr CYP83D1p {Glycine max}PIR|T05940|T05940 TC79302 AI895521 cLEC9E21 IIG2 T1M4 R21 C13 r1-c2 r3-c3 cytochrome P450 83D1p-soybean (fragment) mas-binding factor MBF2 = transcription factor TGA1a TC79327 BF114202 cLEY25L20 XIVC3 T4E6 R19 C5 r2-c2 r1-c4 homolog {Solanum tuberosum = potatoes, root, Peptid cytochrome P450 {Arabidopsis thaliana} TC79360 AI898424 cLED33I8 IIIG3 T1N5 R20 C14 r1-c2 r3-c3 invertase inhibitor homolog {Nicotiana TC79368 AW621436 cLEX11P22 XIIIB8 T4C15 R20 C3 r2-c2 C r1-c4 tabacum}PIR|T03396|T03396 invertase inhibitor homolog-comm putative cytochrome P450 {Arabidopsis TC79382 BE432605 cLEG9B5 VIIA4 T2B7 R18 C2 r4-c2 r1-c3 thaliana}GP|13877661|gb|AAK43908.1|AF370589_1|AF370589 putati triosephosphate isomerase, cytosolic {Coptis TC79385 AI898957 cLED36B9 IIIH1 T1P1 R24 C16 r1-c2 r3-c3 japonica}SP|P21820|TPIS_COPJA TRIOSEPHOSPHATE ISOMERAS putative ABC transporter; 60211-54925 {Arabidopsis TC79386 AI488366 cLED21K4 IIIC5 T1F9 R16 C6 r1-c2 r3-c3 thaliana}PIR|E96742|E96742 probable ABC transpor tyrosine aminotransferase-like protein {Arabidopsis TC79388 AW221912 cLED19D8 IXD2 T3G3 R22 C7 r2-c1 r4-c3 thaliana} fructose-6-phosphate 2-kinase/fructose-2,6- TC79403 AW651075 cLEI15M10 VIIC8 T2F15 R12 C6 r4-c2 r1-c3 bisphosphatase {Solanum tuberosum}PIR|T07016|T07016 6-ph putative glycerol-3-phosphate dehydrogenase TC79406 AW219948 cLEX6M3 XIIIF3 T4K5 R20 C11 r2-c2 r1-c4 {Arabidopsis thaliana} putative cytochrome P450 {Oryza sativa} TC79461 AW219566 cLEX4P4 XIIIE9 T4I17 R8 C9 r2-c2 r1-c4 cytochrome P450 {Arabidopsis thaliana} TC79463 AW160267 cLPT1K21 XVH10 T4P19 R6 C16 r2-c2 r1-c4 anthranilate synthase alpha subunit {Catharanthus TC79471 AW218352 cLEZ7H6 XIVG5 T4M10 R15 C13 r2-c2 r1-c4 roseus} homeodomain protein {Malus x domestica} TC79485 AW737981 cTOD4J4 XVIIH4 T5O7 R18 C15 r3-c2 r4-c4 ferredoxin--nitrite reductase (EC 1.7.7.1) nir-3- TC79488 AI776122 cLER17B5 IXH1 T3O1 R24 C15 r2-c1 r4-c3 common tobacco (fragment) putative sugar transporter {Arabidopsis thaliana} TC79538 AW979980 cLEW10M17 XIID4 T3H8 R17 C8 r2-c1 r4-c3 transcription factor-like protein {Arabidopsis thaliana} TC79544 AW624235 cTOB15G6 XVIIA3 T5A5 R20 C1 r3-c2 r4-c4 Similar to UTP-glucose glucosyltransferases TC79554 AW979370 cLEW1O16 XIIF11 T3L22 R3 C12 r2-c1 r4-c3 {Arabidopsis thaliana}PIR|G86144|G86144 hypothetical pr RING finger protein {Arabidopsis TC79564 AA824862 CT149 XVIC9 T4F18 R7 C6 r2-c2 r1-c4 thaliana}GP|4689366|gb|AAD27870.1|AF134155_1|AF134155 RING finger hexokinase TC79603 AI487152 cLED9E12 XXIIA10 T6A20 R5 C1 r3-c1 r2-c4 starch-branching enzyme-like protein {Arabidopsis TC79638 BG128764 cTOF22C16 XIXE7 T5J13 R12 C10 r3-c2 r4-c4 thaliana} formyltransferase purU homolog {Arabidopsis TC79642 AW399253 cLPT6B20 XVIB6 T4D12 R13 C4 r2-c2 r1-c4 thaliana}GP|2245095|emb|CAB10517.1||Z97343 formyltransf putative heat shock transcription factor {Arabidopsis TC79646 AI637387 DB#357 XXG11 T5N22 R3 C14 r3-c2 r4-c4 thaliana}PIR|T02609|T02609 probable heat shoc Identical to A. thaliana Myb-like protein (gb|D58424). TC79650 AW625194 cLEZ11M12 XIVD2 T4G4 R21 C7 r2-c2 r1-c4 {Arabidopsis thaliana}PIR|F86231|F86231 hypo nucleoside diphosphate kinase {Pisum sativum} TC79659 AW219287 cLEX3P2 XIIIE4 T4I7 R18 C9 r2-c2 r1-c4 putative C3HC4-type RING zinc finger/ankyrin protein TC79668 AW651244 cLEI16E1 VIIC10 T2F19 R6 C6 r4-c2 r1-c3 {Arabidopsis thaliana}PIR|E84689|E84689 probab isopentenyl diphosphate isomerase 1 {Nicotiana TC79669 AI899441 cLES11G14 XD3 T3G6 R19 C7 r2-c1 r4-c3 tabacum} vacuolar ATP synthase catalytic subunit a kDa subunit) TC79686 BG133536 cTOE13N13 XVIIIC2 T5E4 R21 C5 r3-c2 r4-c4 {Daucus carota}SP|P09469|VATA_DAUCA VACUOLAR zinc-finger-like protein {Arabidopsis TC79692 AI780412 cLES11N11 XD5 T3G10 R15 C7 r2-c1 r4-c3 thaliana}PIR|T45654|T45654 zinc-finger-like protein- Arabido phaseolin G-box binding protein PG1 {Phaseolus TC79707 AW622187 cLEX14B17 XIIIC7 T4E13 R12 C5 r2-c2 r1-c4 vulgaris}GP|1142619|gb|AAB00686.1||U18348 phaseolin ALTERNATIVE OXIDASE 1 PRECURSOR (EC 1.—.—. TC79757 BE449757 cLEY14E21 XIIIG5 T4M9 R16 C13 r2-c2 r1-c4 —).GP|558054|gb|AAC60576.1||S71335 alternative oxidase, A dTDP-glucose 4-6-dehydratase-like protein TC79798 AW035334 cLEC40J6 IID7 T1G14 R11 C7 r1-c2 r3-c3 {Arabidopsis thaliana}PIR|T45892|T45892 dTDP- glucose 4-6- flavonol 3-o-glucosyltransferase 6 {Manihot TC79809 AW219975 cLEX6O3 XIIIF6 T4K11 R14 C11 r2-c2 r1-c4 esculenta}SP|Q40288|UFO6_MANES FLAVONOL 3- O-GLUCOSYLTRA soluble starch (bacterial glycogen) synthase {Solanum TC79837 AW398573 cLPT2F24 XVIA3 T4B6 R19 C2 r2-c2 r1-c4 tuberosum}SP|P93568|UGS2_SOLTU SOLUBLE GLYCOG lipoxygenase {Lycopersicon TC79855 BG627392 cLEL17E23 XXIC10 T6E19 R6 C5 r3-c1 r2-c4 esculentum}GP|1654138|gb|AAB65766.1||U37839 lipoxygenase {Lycopersicon e alpha-glucosidase {Solanum TC79865 AW442724 cLET41J16 XIIA2 T3B4 R21 C2 r2-c1 r4-c3 tuberosum}PIR|T07391|T07391 probable alpha- glucosidase (EC 3.2.1.20)-p putative tyrosine decarboxylase {Arabidopsis TC79868 AI898611 cLED34F18 IIIG7 T1N13 R12 C14 r1-c2 r3-c3 thaliana}PIR|A84588|A84588 probable tyrosine decarboxy CYTOCHROME P450 83B1 (EC 1.14.—.—). TC79908 AW038144 cLET1B18 XIE5 T3J9 R16 C10 r2-c1 r4-c3 GP|3164126|dbj|BAA28531.1||D78598 cytochrome P450 monooxygenase lipoxygenase {Solanum TC79919 BG128802 cTOF22I24 XIXF1 T5L1 R24 C12 r3-c2 r4-c4 tuberosum}GP|1117793|gb|AAD09202.1||U24232 lipoxygenase {Solanum tuberosum}P putative ABC transporter; 73228-76244 {Arabidopsis TC79941 AW442122 cLEN21M4 IXC2 T3E3 R22 C5 r2-c1 r4-c3 thaliana} cytochrome p450 lxxviia2 {Solanum TC79994 AI779498 cLES8M17 XIB2 T3D3 R22 C4 r2-c1 r4-c3 melongena}SP|P37124|C772_SOLME CYTOCHROME P450 77A2 (EC 1.14.—.—) ARF GAP-like zinc finger-containing protein ZiGA4 TC80002 AW399699 cLPT8B12 XVIC2 T4F4 R21 C6 r2-c2 r1-c4 {Arabidopsis thaliana} auxin-induced basic helix-loop-helix transcription TC80007 BG127646 cTOF17M2 XIXB6 T5D11 R14 C4 r3-c2 r4-c4 factor, putative {Arabidopsis thaliana}GP|123213 contains similarity to limonene TC80009 AW442145 cLEN21D5 IXB11 T3C21 R4 C3 r2-c1 r4-c3 cyclase~gene_id: K15O15.2 {Arabidopsis thaliana} CYTOCHROME P450 90A1 (EC 1.14.—.—). TC80029 BG631306 cLEL7D21 XXH9 T5P18 R7 C16 r3-c2 r4-c4 GP|853719|emb|CAA60793.1||X87367 CYP90 protein {Arabidopsis thal CYTOCHROME P450 84A1 (FERULATE-5- TC80030 AI780540 cLES12C18 XD7 T3G14 R11 C7 r2-c1 r4-c3 HYDROXYLASE) (EC 1.14.—.—) (F5H).GP|1488255|gb|AAC49389.1||U38416 transcription factor RUSH-1alpha isolog; 18684-24052 TC80033 BG630066 cLEL31A17 XXIH7 T6O13 R12 C15 r3-c1 r2-c4 {Arabidopsis thaliana}PIR|A86245|A86245 hypoth FLAVONOID 3′,5′-HYDROXYLASE (EC 1.14.—.—) TC80085 AW030933 cLEC5M11 IIE2 T1I4 R21 C9 r1-c2 r3-c3 (F3′5′H) (CYTOCHROME P450 75A4).GP|1620009|dbj|BAA12735.1 76 kDa mitochondrial complex I subunit {Solanum TC80110 BG642432 cTOD11I5 XVH2 T4P3 R22 C16 r2-c2 r1-c4 tuberosum}SP|Q43644|NUAM_SOLTU NADH- UBIQUINONE OXID ABC transporter homolog {Populus nigra} TC80115 BF096365 cLEW11G12 XIID5 T3H10 R15 C8 r2-c1 r4-c3 Contains similarity to 12S seed storage globulin TC80151 BG628122 cLEL20G15 XXIE4 T6I7 R18 C9 r3-c1 r2-c4 precursor GP|134919. ESTs gb|T13642, gb|T21684 and decarboxylase like protein {Arabidopsis TC80187 BE451597 cLEY20L7 XIVB6 T4C12 R13 C3 r2-c2 r1-c4 thaliana}GP|2245025|emb|CAB10445.1||Z97341 decarboxylase li aldose-1-epimerase-like protein {Nicotiana TC80210 AI775211 cLER14J20 IXF5 T3K9 R16 C11 r2-c1 r4-c3 tabacum}PIR|T01933|T01933 probable aldose 1- epimerase (E ATP synthase alpha subunit, mitochondrial {Nicotiana TC80243 AW929036 cTOC3L1 XVIID7 T5G13 R12 C7 r3-c2 r4-c4 plumbaginifolia}SP|P05495|ATP0_NICPL ATP SYNTH cytochrome p450 lxxia2 {Solanum TC80252 AW034502 cLEC24A10 IF4 T1K7 R18 C11 r1-c2 r3-c3 melongena}SP|P37118|C712_SOLME CYTOCHROME P450 71A2 (EC 1.14.—.—) ( CYTOCHROME P450 71A22 (EC 1.14.—.—). TC80253 AW032176 cLEC20M3 IE4 T1I7 R18 C9 r1-c2 r3-c3 GP|4678357|emb|CAB41167.1||AL049659 cytochrome P450-like protei putative dehydroquinase shikimate dehydrogenase TC80290 AI779843 cLES9G4 XIB7 T3D13 R12 C4 r2-c1 r4-c3 {Arabidopsis thaliana} homogentisate 1,2-dioxygenase {Lycopersicon TC80293 AW092200 cLET17L20 IB3 T1C5 R20 C3 r1-c2 r3-c3 esculentum} general negative transcription regulator-like TC80302 AW399344 cLPT7O15 XVIC1 T4F2 R23 C6 r2-c2 r1-c4 {Arabidopsis thaliana} putative transcriptional co-activator {Arabidopsis TC80320 AI779030 cLES6L18 XIA5 T3B9 R16 C2 r2-c1 r4-c3 thaliana}GP|3513735|gb|AAC33951.1||AF080118 cont putative cytochrome P450 TC80358 BG131093 cTOE2F5 XVIIIF1 T5K2 R23 C11 r3-c2 r4-c4 phospho-2-dehydro-3-deoxyheptonate aldolase TC80361 AI897267 cLED26J15 IIID10 T1H19 R6 C8 r1-c2 r3-c3 glyceraldehyde 3-phosphate dehydrogenase a precursor, TC80364 AW428960 cTOA2K2 XVIE10 T4J20 R5 C10 r2-c2 r1-c4 chloroplast {Nicotiana tabacum}SP|P09043|G3PA aminomethyltransferase precursor system t protein) TC80365 BG127639 cTOF17K6 XIXB5 T5D9 R16 C4 r3-c2 r4-c4 {Solanum tuberosum}SP|P54260|GCST_SOLTU AMINOMET glyceraldehyde 3-phosphate dehydrogenase a precursor, TC80366 BE434460 cLEG17I17 VF5 T2K9 R16 C11 r4-c2 r1-c3 chloroplast {Nicotiana tabacum}SP|P09043|G3PA hydroxymethyltransferase {Arabidopsis TC80391 BG135712 cTOE23K18 XVIIIE9 T5I18 R7 C9 r3-c2 r4-c4 thaliana}GP|2244749|emb|CAB10172.1||Z97335 hydroxymethyltrans hydroxymethyltransferase {Arabidopsis TC80394 BG130817 cTOE1I22 XVIIID10 T5G20 R5 C7 r3-c2 r4-c4 thaliana}GP|2244749|emb|CAB10172.1||Z97335 hydroxymethyltrans putative fructose-bisphosphate aldolase, plastidic form TC80401 AI895082 cLEC6B14 IIE4 T1I8 R17 C9 r1-c2 r3-c3 {Arabidopsis thaliana}GP|11762176|gb|AAG403 ATP synthase delta' subunit, mitochondrial precursor TC80407 BE450930 cLEY15P13 XIIIH11 T4O21 R4 C15 r2-c2 r1-c4 {Ipomoea batatas}SP|Q40089|ATP4_IPOBA ATP SYNT glyceraldehyde 3-phosphate dehydrogenase TC80408 AI775098 cLER14D11 IXF2 T3K3 R22 C11 r2-c1 r4-c3 S-adenosyl-L-methionine synthetase TC80422 AW221689 cLEN3H21 IXC6 T3E11 R14 C5 r2-c1 r4-c3 S-adenosyl-L-methionine synthetase TC80423 BG123796 cTOF3K21 XXE1 T5J2 R23 C10 r3-c2 r4-c4 S-adenosylmethionine synthase 3 {Lycopersicon TC80424 BF051914 cLEM24J5 VIIIC7 T2F14 R11 C6 r4-c2 r1-c3 esculentum}SP|P43282|METM_LYCES S- ADENOSYLMETHIONINE cystathionine gamma-synthase isoform 1 {Solanum TC80427 BE433564 cLEG16E12 VC11 T2E21 R4 C5 r4-c2 r1-c3 tuberosum} acetyl-CoA acyltransferase {Cucumis TC80431 AW648018 cLEN15N9 VIID12 T2H23 R2 C8 r4-c2 r1-c3 sativus}GP|393707|emb|CAA47926.1||X67696 acetyl- CoA acyltransf xylose isomerase {Hordeum TC80432 AW928693 cTOC2F20 XVIID4 T5G7 R18 C7 r3-c2 r4-c4 vulgare}SP|Q40082|XYLA_HORVU XYLOSE ISOMERASE (EC 5.3.1.5).GP|1296809|em cytochrome P450 {Arabidopsis thaliana} TC80453 AI484770 cLED3B5 IIIH11 T1P21 R4 C16 r1-c2 r3-c3 Contains a PF|00175 Oxidoreductase FAD/NADH- TC80456 BE434351 cLEG16M23 VF3 T2K5 R20 C11 r4-c2 r1-c3 binding domain. ESTs gb|H76345 and gb|AA651465 come fro caffeoyl-coenzymeA O-methyltransferase {Nicotiana TC80468 AW040773 cLET10L1 XIC4 T3F7 R18 C6 r2-c1 r4-c3 tabacum}GP|1574946|gb|AAC49913.1||U38612 caffeoyl homologous to GATA-binding transcription factors TC80486 AW929937 cTOC8K12 XVIIF2 T5K3 R22 C11 r3-c2 r4-c4 {Arabidopsis thaliana}GP|7288001|emb|CAB81839.1||A NADP-malic enzyme{circumflex over ( )}{circumflex over ( )}malate dehydrogenase TC80499 AW616604 cLHT11H20 XIVH6 T4O12 R13 C15 r2-c2 r1-c4 MADS box transcription factor-like {Arabidopsis TC80500 BG123322 cTOF1H5 XIXD4 T5H7 R18 C8 r3-c2 r4-c4 thaliana} triosephosphate isomerase, cytosolic {Petunia TC80531 BG125992 cTOF10J13 XXID10 T6G19 R6 C7 r3-c1 r2-c4 hybrida}SP|P48495|TPIS_PETHY TRIOSEPHOSPHATE ISOMERAS putative homeodomain transcription factor {Arabidopsis TC80540 AI490360 cLED15E8 IIIA3 T1B5 R20 C2 r1-c2 r3-c3 thaliana}PIR|H84774|H84774 probable homeodom malate dehydrogenase {Nicotiana tabacum} TC80550 AI775216 cLER14L14 XIIB3 T3D6 R19 C4 r2-c1 r4-c3 bZIP DNA-binding protein TC80553 BF051949 cLEM24B20 VIIIC1 T2F2 R23 C6 r4-c2 r1-c3 lysine-ketoglutarate reductase/saccharopine TC80556 AI894874 cLEC6K9 IIE10 T1I20 R5 C9 r1-c2 r3-c3 dehydrogenase bifunctional enzyme {Arabidopsis thaliana} phosphoglycerate kinase precursor {Solanum TC80567 AI774923 cLER13F4 XID3 T3H5 R20 C8 r2-c1 r4-c3 tuberosum}PIR|T07014|T07014 phosphoglycerate kinase (EC proton pump interactor {Arabidopsis TC80570 AW441201 cLEN4D17 IXC8 T3E15 R12 C5 r2-c1 r4-c3 thaliana}GP|7269604|emb|CAB81400.1||AL161571 proton pump intera malate dehydrogenase {Glycine max} TC80572 BF098428 cLEW27A2 IB2 T1C3 R22 C3 r1-c2 r3-c3 NADH-ubiquinone oxidoreductase 20 kDa subunit TC80576 BE436586 cLEG33O5 VIB11 T2C22 R3 C3 r4-c2 r1-c3 precursor {Solanum tuberosum}SP|Q43844|NUKM_SOLTU NAD MADS-box transcription factor FBP5 {Petunia x TC80582 BE461808 cLEG40E23 VIE12 T2I24 R1 C9 r4-c2 r1-c3 hybrida} serine hydroxymethyltransferase, mitochondrial TC80593 AI776896 cLER20K5 XB3 T3C6 R19 C3 r2-c1 r4-c3 precursor {Solanum tuberosum}SP|P50433|GLYM_SOLTU SE serine hydroxymethyltransferase, mitochondrial TC80594 AW040297 cLET5K17 XIIB10 T3D20 R5 C4 r2-c1 r4-c3 precursor {Solanum tuberosum}SP|P50433|GLYM_SOLTU SE homeodomain protein TC80595 AI487520 cLED11B1 IIG6 T1M12 R13 C13 r1-c2 r3-c3 homeodomain leucine-zipper protein ATHB13 TC80599 AI486971 cLED6P3 IVC1 T1F2 R23 C6 r1-c2 r3-c3 {Arabidopsis thaliana}GP|12325190|gb|AAG52541.1|AC013289_(—) spermidine synthase {Arabidopsis thaliana} TC80606 BE433027 cLEG11N5 VD8 T2G15 R12 C7 r4-c2 r1-c3 putative ATP synthase {Arabidopsis TC80612 AW649042 cLEI6J24 VIIF6 T2L11 R14 C12 r4-c2 r1-c3 thaliana}PIR|B84606|B84606 probable ATP synthase [imported]-Ar dTDP-glucose 4-6-dehydratases-like protein TC80616 BE461694 cLEG39N23 VIE10 T2I20 R5 C9 r4-c2 r1-c3 {Arabidopsis thaliana}PIR|T45701|T45701 dTDP- glucose 4-6 homology to pyroxidal-5′-phosphate-dependant TC80620 BE434007 cLEG13D11 VID12 T2G24 R1 C7 r4-c2 r1-c3 glutamate decarboxylases; putative start codon glutamate decarboxylase {Lycopersicon TC80621 BE460614 cLEG33E2 VIB7 T2C14 R11 C3 r4-c2 r1-c3 esculentum}SP|P54767|DCE_LYCES GLUTAMATE DECARBOXYLASE (EC 4. osmotic stress-induced zinc-finger protein {Nicotiana TC80630 AW030858 cLEC21H24 IE9 T1I17 R8 C9 r1-c2 r3-c3 tabacum}PIR|T01985|T01985 zinc-finger protein ferritin subunit cowpea2 precursor {Vigna TC80669 BF050399 cLEM17N17 XIIA4 T3B8 R17 C2 r2-c1 r4-c3 unguiculata}PIR|T08124|T08124 ferritin 2 precursor- cowp contains similarity to NADH dehydrogenase chain CI- TC80670 AW625698 cLEZ16F15 XIVD12 T4G24 R1 C7 r2-c2 r1-c4 18~gene_id: K9I9.16 {Arabidopsis thaliana} succinate dehydrogenase TC80679 BG136628 cLPP3O11 XVE11 T4J21 R4 C10 r2-c2 r1-c4 putative glycine decarboxylase p-protein TC80681 AW096471 cLET38N21 XVID4 T4H8 R17 C8 r2-c2 r1-c4 S-ADENOSYLMETHIONINE DECARBOXYLASE TC80692 BG138411 cLPP9K14 XVF7 T4L13 R12 C12 r2-c2 r1-c4 PROENZYME (EC 4.1.1.50) (ADOMETDC) (SAMDC).GP|1498080|gb|AAC0461 CONSTANS-like protein 2 {Malus x domestica} TC80693 AI484848 cLED2N21 IIIE11 T1J21 R4 C10 r1-c2 r3-c3 pyruvate kinase (EC 2.7.1.40), cytosolic-potato TC80694 AW219226 cLEX3K18 XIIIE1 T4I1 R24 C9 r2-c2 r1-c4 ATP synthase delta subunit, mitochondrial precursor TC80699 BG643528 cTOF31E5 XXC3 T5F6 R19 C6 r3-c2 r4-c4 (oligomycin sensitivity conferral protein) (oscp Tetrafunctional protein of glyoxysomal fatty acid beta- TC80702 AI774151 cLER10D22 IXE4 T3I7 R18 C9 r2-c1 r4-c3 oxidation {Brassica napus}PIR|T08017|T08017 PROBABLE VACUOLAR ATP SYNTHASE TC80710 AW441330 cLEN15M17 IXA6 T3A11 R14 C1 r2-c1 r4-c3 SUBUNIT H (EC 3.6.1.34) (V-ATPASE H SUBUNIT) (VACUOLAR PROTON PUMP H Strong similarity to gb|L34684 inosine monophosphate TC80721 AW737443 cTOD2P4 XVIIG6 T5M11 R14 C13 r3-c2 r4-c4 dehydrogenase (IMPDH) from Arabidopsis thaliana phosphate/phosphoenolpyruvate translocator-like TC80730 BG138390 cLPP9C20 XVF6 T4L11 R14 C12 r2-c2 r1-c4 protein {Arabidopsis thaliana} 3-isopropylmalate dehydrogenase precursor TC80800 BE344489 cLEY2O13 XIVC7 T4E14 R11 C5 r2-c2 r1-c4 dehydrogenase) (imdh) (3-ipm-dh) {Solanum tuberosum}SP|P2 sucrose transporter TC80801 AI782568 cLES20C5 XIIA3 T3B6 R19 C2 r2-c1 r4-c3 citrate synthase, glyoxysomal precursor {Cucurbita TC80803 BE437000 cLEG35K15 VIC7 T2E14 R11 C5 r4-c2 r1-c3 maxima}SP|P49299|CYSZ_CUCMA CITRATE SYNTHASE, GL UDP-glucose:protein transglucosylase {Solanum TC80818 BG125578 cTOF9G19 XXG8 T5N16 R9 C14 r3-c2 r4-c4 tuberosum} delta-12 fatty acid desaturase {Borago officinalis} TC80824 BG138370 cLPP9A16 XVF5 T4L9 R16 C12 r2-c2 r1-c4 enoyl-ACP reductase {Petunia x hybrida} TC80834 BE459984 cLEM8J9 VIIIF5 T2L10 R15 C12 r4-c2 r1-c3 Similar to acyl carrier protein, mitochondrial precursor TC80836 AI485151 cLED7G23 IVC4 T1F8 R17 C6 r1-c2 r3-c3 (ACP) NADH-ubiquinone oxidoreductase 9.6 KD omega-3 fatty acid desaturase, endoplasmic reticulum TC80843 BG123845 cTOF3G12 XXD9 T5H18 R7 C8 r3-c2 r4-c4 {Nicotiana tabacum}SP|P48626|FD3E_TOBAC OMEGA- UDP-glucose glucosyltransferase {Arabidopsis TC80847 AW625604 cLEZ15P21 XIVD8 T4G16 R9 C7 r2-c2 r1-c4 thaliana}GP|9392679|gb|AAF87256.1|AC068562_3|AC068562 isocitrate dehydrogenase (NADP+) {Solanum TC80851 AI895979 cLEC13B9 VIF11 T2K22 R3 C11 r4-c2 r1-c3 tuberosum}PIR|T07402|T07402 probable isocitrate dehydroge zinc finger protein {Pisum sativum}PIR|T48868|T48868 TC80860 BG136538 cLPP2N17 XVE9 T4J17 R8 C10 r2-c2 r1-c4 zinc finger protein [imported]-garden pea putative ABC transporter ATPase; 10053-12032 TC80867 BG125731 cTOF9J23 XXG10 T5N20 R5 C14 r3-c2 r4-c4 {Arabidopsis thaliana} transcriptional regulator, putative; 35498-34111 TC80874 BE435682 cLEG28G12 VH6 T2O11 R14 C15 r4-c2 r1-c3 {Arabidopsis thaliana}PIR|H96576|H96576 hypothetic legumin-like protein {Arabidopsis TC80885 AW218154 cLEZ1G23 XIVF7 T4K14 R11 C11 r2-c2 r1-c4 thaliana}PIR|H84687|H84687 legumin-like protein [imported]- Arab ATP:citrate lyase {Capsicum annuum} TC80889 BG128839 cTOF22D3 XIXE9 T5J17 R8 C10 r3-c2 r4-c4 hyoscyamine 6-dioxygenase hydroxylase) {Hyoscyamus TC80893 AW649940 cLEI11O1 VIIA11 T2B21 R4 C2 r4-c2 r1-c3 niger}SP|P24397|HY6H_HYONI HYOSCYAMINE 6- DIOXYGE RING-H2 finger protein RHF2a {Arabidopsis TC80911 AW441998 cLEN19D11 VIH5 T2O10 R15 C15 r4-c2 r1-c3 thaliana}GP|13374859|emb|CAC34493.1||AL589883 RING-H2 fin putative GDP-mannose pyrophosphorylase; 64911-67597 TC80933 AW929477 cTOC9C23 XVIIF4 T5K7 R18 C11 r3-c2 r4-c4 {Arabidopsis thaliana}PIR|G96778|G96778 hypothe glucosyltransferase-like protein {Arabidopsis thaliana} TC80941 AI898616 cLED34H6 IIIG8 T1N15 R12 C14 r1-c2 r3-c3 putative caffeoyl-CoA O-methyltransferase TC80956 BE459185 cLEM5B22 VIIID10 T2H20 R5 C8 r4-c2 r1-c3 {Arabidopsis thaliana} fatty acid elongase-like protein (cer2-like) {Arabidopsis TC80962 BG125978 cTOF10H3 XE2 T3I4 R21 C9 r2-c1 r4-c3 thaliana}GP|7268088|emb|CAB78426.1||AL161 TOM (target of myb1)-like protein {Arabidopsis TC80976 AW616929 cLHT18D23 XVA5 T4B9 R16 C2 r2-c2 r1-c4 thaliana}PIR|T51543|T51543 TOM (target of myb1)- like heat shock transcription factor-like protein {Arabidopsis TC80978 AI489721 cLED15A9 IIH11 T1O22 R3 C15 r1-c2 r3-c3 thaliana} Similar to ATP-citrate-lyase {Arabidopsis TC80979 AI771253 cLED28P7 IIIE5 T1J9 R16 C10 r1-c2 r3-c3 thaliana}PIR|F86227|F86227 hypothetical protein [imported putative NADH-ubiquinone oxireductase {Arabidopsis TC80984 BF098069 cLEW25M9 XIIG10 T3N20 R5 C14 r2-c1 r4-c3 thaliana}PIR|C84588|C84588 probable NADH-ubiquin putative deoxycytidylate deaminase {Cicer arietinum} TC80988 AI772030 cLER1O18 XA11 T3A22 R3 C1 r2-c1 r4-c3 putative RING finger protein; 84236-82024 TC81001 BE461509 cLEG39A11 VIE6 T2I12 R13 C9 r4-c2 r1-c3 {Arabidopsis thaliana}PIR|A96829|A96829 probable RING fin putative RING finger protein; 84236-82024 TC81002 AW648088 cLEI3K12 VIID10 T2H19 R6 C8 r4-c2 r1-c3 {Arabidopsis thaliana}PIR|A96829|A96829 probable RING fin RING finger-like protein {Arabidopsis TC81013 AI489945 cLED14K18 IIH10 T1O20 R5 C15 r1-c2 r3-c3 thaliana}PIR|T47595|T47595 RING finger protein T12E18.50-Ar mevalonate diphosphate decarboxylase {Arabidopsis TC81015 BF051253 cLEM22C23 VIIIA10 T2B20 R5 C2 r4-c2 r1-c3 thaliana}GP|3250736|emb|CAA76803.1||Y17593 mevalo aspartate aminotransferase {Oryza TC81020 BE432751 cLEG10K11 VD6 T2G11 R14 C7 r4-c2 r1-c3 sativa}PIR|JC5125|JC5125 aspartate transaminase (EC 2.6.1.1) prec NADP-dependent isocitrate dehydrogenase-like protein TC81025 AW651062 cLEI15I20 VIIC6 T2F11 R14 C6 r4-c2 r1-c3 Strong similarity to F19I3.8 GP|3033381 putative UDP- TC81034 AW033767 cLEC29E1 XXIE10 T6I19 R6 C9 r3-c1 r2-c4 galactose-4-epimerase from Arabidopsis thaliana glucosyltransferase-like protein {Arabidopsis thaliana} TC81042 AW039906 cLET13B22 IA4 T1A7 R18 C1 r1-c2 r3-c3 omega-6 fatty acid desaturase, chloroplast precursor TC81045 AW399600 cLPT8K1 XVIC5 T4F10 R15 C6 r2-c2 r1-c4 {Brassica napus}SP|P48627|FD6C_BRANA OMEGA-6 F acyl-ACP thioesterase {Garcinia mangostana} TC81091 AI489140 cLED15I7 XVIIH5 T5O9 R16 C15 r3-c2 r4-c4 ATP synthase a subunit precursor {Nicotiana TC81098 AI898457 cLED34E17 IIIG6 T1N11 R14 C14 r1-c2 r3-c3 tabacum}SP|P06288|ATPI_TOBAC ATP SYNTHASE A CHAIN PRECU 3-isopropylmalate dehydrogenase precursor TC81104 AW928771 cTOC3E9 VD7 T2G13 R12 C7 r4-c2 r1-c3 dehydrogenase) (imdh) (3-ipm-dh) {Brassica napus}SP|P2910 anthranilate N-benzoyltransferase {Arabidopsis TC81105 AW625953 cLEZ17P13 XIVE8 T4I16 R9 C9 r2-c2 r1-c4 thaliana} cytochrome c oxidase subunit Vb precursor-like protein TC81111 AW039677 cLET13C21 XIC9 T3F17 R8 C6 r2-c1 r4-c3 {Arabidopsis thaliana} UMP synthase {Nicotiana plumbaginifolia} TC81117 BG130029 cTOF29I5 XVIG8 T4N16 R9 C14 r2-c2 r1-c4 anthocyanin 5-O-glucosyltransferase {Petunia x TC81118 BG135580 cTOE23C9 XVIIIE8 T5I16 R9 C9 r3-c2 r4-c4 hybrida} uridine kinase-like protein {Arabidopsis thaliana} TC81123 AW928947 cTOC4E6 XVIC8 T4F16 R9 C6 r2-c2 r1-c4 putative homeodomain transcription factor {Arabidopsis TC81124 BG129304 cTOF23N12 XIXG3 T5N5 R20 C14 r3-c2 r4-c4 thaliana}PIR|H84774|H84774 probable homeodom glucose-regulated protein 78 TC81129 AW650486 cLEI13M5 XVIIH2 T5O3 R22 C15 r3-c2 r4-c4 contains similarity to acyl-CoA TC81143 AI486923 cLED6D7 IVB5 T1D10 R15 C4 r1-c2 r3-c3 thioesterase~gene_id: K23F3.9 {Arabidopsis thaliana} HOMEOBOX-LEUCINE ZIPPER PROTEIN HAT5 TC81154 AW623618 cTOB11B23 XVIF11 T4L22 R3 C12 r2-c2 r1-c4 (HD-ZIP PROTEIN 5) (HD-ZIP PROTEIN ATHB- 1).□GP|16329|emb|CAA416 phosphoenolpyruvate carboxylase 1 {Gossypium TC81155 BG62607 cPP1O21 XXIA5 T6A9 R16 C1 r3-c1 r2-c4 hirsutum}GP|2266947|gb|AAB80714.1||AF008939 phosphoeno transcription factor CRC {Arabidopsis TC81170 AI485831 cLED4O9 IVA9 T1B18 R7 C2 r1-c2 r3-c3 thaliana}GP|12325076|gb|AAG52485.1|AC018364_3|AC018364 transc putative glucose regulated repressor protein TC81176 BE433829 cLEG7F16 XIIF3 T3L6 R19 C12 r2-c1 r4-c3 {Arabidopsis thaliana}PIR|A84649|A84649 probable gluco cytochrome P450 {Nicotiana TC81178 AW737552 cTOD3H13 XVIG9 T4N18 R7 C14 r2-c2 r1-c4 tabacum}GP|1237250|emb|CAA65580.1||X96784 cytochrome P450 {Nicotiana tab tryptophan synthase alpha 1-like protein {Arabidopsis TC81185 BE460501 cLEG31J1 VIA9 T2A18 R7 C1 r4-c2 r1-c3 thaliana}GP|3892048|gb|AAC78257.1|AAC78257|AC small zinc finger-like protein TC81193 BG127265 cTOF14N18 XIXA5 T5B9 R16 C2 r3-c2 r4-c4 MybSt1 {Solanum tuberosum} TC81223 AW091869 cLET16L16 XID7 T3H13 R12 C8 r2-c1 r4-c3 immediate-early salicylate-induced glucosyltransferase TC81244 BE434667 cLEG20E17 VG2 T2M3 R22 C13 r4-c2 r1-c3 {Nicotiana tabacum}GP|1685005|gb|AAB36653.1| bZIP transcription factor {Nicotiana tabacum} TC81272 AW738717 cTOD8G2 XVIIIB1 T5C2 R23 C3 r3-c2 r4-c4 aspartate aminotransferase, cytoplasmic {Daucus TC81279 BF052193 cLEM25L10 VIIIC10 T2F20 R5 C6 r4-c2 r1-c3 carota}SP|P28734|AATC_DAUCA ASPARTATE AMINOTRANSFER putative RING zinc finger protein; 53384-54880 TC81280 AI896388 cLEC15M17 ID8 T1G15 R12 C7 r1-c2 r3-c3 {Arabidopsis thaliana}PIR|G96835|G96835 probable RIN similar to ATPases associated with various cellular TC81288 AI775557 cLER15L4 IXF12 T3K23 R2 C11 r2-c1 r4-c3 activites (Pfam: AAA.hmm, score: 230.91) {Arabid ASPARTATE AMINOTRANSFERASE, TC81293 BG125276 cTOF8K11 XXG5 T5N10 R15 C14 r3-c2 r4-c4 MITOCHONDRIAL PRECURSOR (EC 2.6.1.1) (TRANSAMINASE A).GP|531555|emb|CAA phosphoribosylanthranilate transferase {Arabidopsis TC81302 BE460055 cLEM8H10 VIIIF3 T2L6 R19 C12 r4-c2 r1-c3 thaliana} D-ribulose-5-phosphate 3-epimerase {Oryza sativa} TC81304 AW223738 cLEN13B9 VIIIH2 T2P4 R21 C16 r4-c2 r1-c3 malate dehydrogenase, glyoxysomal precursor TC81324 AW647654 cLEI10F3 VIIA9 T2B17 R8 C2 r4-c2 r1-c3 {Citrullus vulgaris}EGAD|130842|139627 glyoxysomal mala glyceraldehyde 3-phosphate dehydrogenase, cytosolic TC81336 BG135725 cTOE23M22 XVG10 T4N19 R6 C14 r2-c2 r1-c4 {Petunia hybrida}SP|P26520|G3PC_PETHY GLYCERALD CCAAT-binding transcription factor subunit A(CBF-A) TC81341 AI782351 cLES18L2 IVG7 T1N14 R11 C14 r1-c2 r3-c3 {Arabidopsis thaliana}GP|2244810|emb|CAB10233.1 H+-transporting ATPase-like protein {Arabidopsis TC81342 AW650530 cLEI13E8 VIIB9 T2D17 R8 C4 r4-c2 r1-c3 thaliana}GP|7270157|emb|CAB79970.1||AL161581 H+- tr ZF-HD homeobox protein {Flaveria bidentis} TC81347 BG643218 cTOF26N24 XIXH12 T5P23 R2 C16 r3-c2 r4-c4 PUTATIVE NADH-UBIQUINONE TC81349 AW038388 cLET5I16 XIIB9 T3D18 R7 C4 r2-c1 r4-c3 OXIDOREDUCTASE SUBUNIT B17.2 (EC 1.6.5.3) (EC 1.6.99.3) (COMPLEX I-B17.2) ( SNF5, transcription regulatory protein homolog BSH TC81352 AI898634 cLED34L6 IIIG9 T1N17 R8 C14 r1-c2 r3-c3 {Arabidopsis thaliana} putative glucosyltransferase {Arabidopsis TC81356 AW648029 cLEI3O7 VIIE3 T2J5 R20 C10 r4-c2 r1-c3 thaliana}GP|4309698|gb|AAD15482.1||AC006266 putative gluc glutamine cyclotransferase precursor {Carica TC81367 AI897111 cLED26K16 XIVA8 T4A16 R9 C1 r2-c2 r1-c4 papaya}PIR|T08168|T08168 glutaminyl-peptide cyclotrans contains similarity to sugar transporters (Pfam: TC81373 BG137973 cLPP7N18 XVF3 T4L5 R20 C12 r2-c2 r1-c4 sugar_tr.hmm, score: 395.91) {Arabidopsis thaliana} putative folylpolyglutamate synthetase {Oryza sativa} TC81390 BE433834 cLEG7H4 VIH8 T2O16 R9 C15 r4-c2 r1-c3 S-adenosyl-L-methionine Mg-protoporphyrin IX TC81391 BG126969 cTOF14A13 XVIIIH12 T5O24 R1 C15 r3-c2 r4-c4 methyltranserase {Nicotiana tabacum} contains similarity to ATP synthase B/B′ (Pfam: ATP- TC81399 BF051056 cLEM21O2 XVH11 T4P21 R4 C16 r2-c2 r1-c4 synt_B.hmm, score: 11.71) {Arabidopsis thaliana} Contains similarity to gb|AJ006354 zinc finger protein TC81419 AW442254 cLEN22G16 IXC4 T3E7 R18 C5 r2-c1 r4-c3 (ZAC) from Homo sapiens. {Arabidopsis thalian dihydroflavonol 4-reductase-like {Arabidopsis thaliana} TC81435 BE435324 cLEG26A9 VC5 T2E9 R16 C5 r4-c2 r1-c3 putative RING zinc finger protein {Arabidopsis TC81454 AI488438 cLED21N23 XVIIG7 T5M13 R12 C13 r3-c2 r4-c4 thaliana} beta-amylase {Arabidopsis thaliana} TC81481 AW650286 cLEI12H7 XXH12 T5P24 R1 C16 r3-c2 r4-c4 zinc finger-like protein {Arabidopsis TC81513 BG130666 cTOF31H2 XIVG2 T4M4 R21 C13 r2-c2 r1-c4 thaliana}PIR|T49033|T49033 zinc finger-like protein- Arabido putative methylmalonate semi-aldehyde dehydrogenase TC81537 AW625535 cLEZ15D3 XIVD6 T4G12 R13 C7 r2-c2 r1-c4 {Arabidopsis thaliana}PIR|H84514|H84514 hypothe myb-related protein 340-garden snapdragon TC81538 AI897784 cLED30L23 IIIF8 T1L15 R12 C12 r1-c2 r3-c3 ISOCITRATE DEHYDROGENASE [NADP] (EC TC81566 BE432917 cLEG10H23 XVID12 T4H24 R1 C8 r2-c2 r1-c4 1.1.1.42) (OXALOSUCCINATE DECARBOXYLASE) (IDH) (NADP+-SPECIFIC I UTP-glucose glucosyltransferase-like protein TC81577 BF113450 cLEG44N2 VIG9 T2M18 R7 C13 r4-c2 r1-c3 {Arabidopsis thaliana}GP|4835225|emb|CAB42903.1||AL049 flavanone 3beta-hydroxylase {Petunia x hybrida} TC81579 BE449565 cLHT32A3 XVIE12 T4J24 R1 C10 r2-c2 r1-c4 pyruvate kinase {Arabidopsis thaliana} TC81587 BE353438 cTOA19M23 XVIE6 T4J12 R13 C10 r2-c2 r1-c4 serine hydroxymethyltransferase, mitochondrial TC81590 BF098334 cLEW26O3 XIIH1 T3P2 R23 C16 r2-c1 r4-c3 precursor {Solanum tuberosum}SP|P50433|GLYM_SOLTU SE serine hydroxymethyltransferase, mitochondrial TC81591 BE431621 cLEG30A5 VIA1 T2A2 R23 C1 r4-c2 r1-c3 precursor {Solanum tuberosum}SP|P50433|GLYM_SOLTU SE biotin carboxylase subunit {Nicotiana TC81634 AI483969 cLED23C19 IIIC9 T1F17 R8 C6 r1-c2 r3-c3 tabacum}GP|870726|gb|AAC41659.1||L38260 biotin carboxylase su ornithine carbamoyltransferase {Pisum TC81652 AW093198 cLET24A15 XIF5 T3L9 R16 C12 r2-c1 r4-c3 sativum}SP|Q43814|OTC_PEA ORNITHINE CARBAMOYLTRANSFERASE PREC phosphoenolpyruvate carboxylase kinase {Lycopersicon TC81676 AW442172 cLEN21B14 IXB10 T3C19 R6 C3 r2-c1 r4-c3 esculentum} UDP-glucose glucosyltransferase {Solanum TC81688 AW217408 cTOA6A11 XVIF3 T4L6 R19 C12 r2-c2 r1-c4 tuberosum}GP|1857447|gb|AAB48444.1||U82367 UDP- glucose glu Strong similarity to UDP-glucose glucosyltransferase TC81690 AW033397 cLEC30E24 IH4 T1O7 R18 C15 r1-c2 r3-c3 from Arabidopsis thaliana gb|AB016819 and conta transcription factor NF-Y, CCAAT-binding-like protein TC81698 AW738727 cTOD8G22 XVIIIB2 T5C4 R21 C3 r3-c2 r4-c4 {Arabidopsis thaliana}PIR|T45874|T45874 trans malate dehydrogenase (NADP), chloraplast precursor TC81700 BE432974 cLEG11O15 VD9 T2G17 R8 C7 r4-c2 r1-c3 (NADp-mdh) {Pisum sativum}SP|P21528|MDHC_PEA MAL acyl-CoA:1-acylglycerol-3-phosphate acyltransferase TC81716 AW944886 cTOB12O24 XVIH2 T4P4 R21 C16 r2-c2 r1-c4 {Arabidopsis thaliana} VACUOLAR ATP SYNTHASE SUBUNIT G 2 (EC TC81726 BG131668 cTOE4L10 XVIIIF8 T5K16 R9 C11 r3-c2 r4-c4 3.6.1.34) (V-ATPASE G SUBUNIT 2) (VACUOLAR PROTON PUMP G SUBUN MADS-box transcription factor jointless TC81749 AI895411 cLEC7P7 IIF4 T1K8 R17 C11 r1-c2 r3-c3 putative RING zinc finger protein; 27623-28978 TC81762 AI782511 cLES19H15 XF12 T3K24 R1 C11 r2-c1 r4-c3 {Arabidopsis thaliana}PIR|H96703|H96703 probable RIN Strong similarity to MRP-like ABC transporter TC81773 AI489515 cLED16O3 IIIA11 T1B21 R4 C2 r1-c2 r3-c3 gb|U92650 from A. thaliana and canalicular multi-drug alanine aminotransferase {Arabidopsis thaliana} TC81776 BE433936 cLEG9A20 VIIA3 T2B5 R20 C2 r4-c2 r1-c3 starch synthase, isoform V {Vigna unguiculata} TC81835 BF051825 cLEM24H9 VIIIC5 T2F10 R15 C6 r4-c2 r1-c3 ribulosebisphosphate carboxylase large subunit TC81850 AI486088 cLED5M17 IVB2 T1D4 R21 C4 r1-c2 r3-c3 acetyl-coA dehydrogenase, putative {Arabidopsis TC81857 AW031602 cLEC34G18 IIA8 T1A16 R9 C1 r1-c2 r3-c3 thaliana} MADS box transcription factor MADS1 {Capsicum TC81862 BE436905 cLEG34H13 VIC2 T2E4 R21 C5 r4-c2 r1-c3 annuum} tyrosine aminotransferase-like protein {Arabidopsis TC81863 AW928458 cTOC1D7 XVIID1 T5G1 R24 C7 r3-c2 r4-c4 thaliana} putative RING-H2 zinc finger protein ATL6 TC81880 AW223116 cLEN10F7 XIIIE3 T4I5 R20 C9 r2-c2 r1-c4 {Arabidopsis thaliana} dihydrodipicolinate synthase {Nicotiana TC81883 AW623776 cTOB13I5 XVIH6 T4P12 R13 C16 r2-c2 r1-c4 tabacum}SP|Q42948|DAPA_TOBAC DIHYDRODIPICOLINASE SYNTHASE P putative CTP synthase {Oryza sativa) TC81887 AW035658 cLEC34D4 IIA7 T1A14 R11 C1 r1-c2 r3-c3 transcription factor-like; similar to CH6 and COP9 TC81893 BE353981 cTOD8B20 XVIIIA11 T5A22 R3 C1 r3-c2 r4-c4 complex subunit 6 {Arabidopsis thaliana} putative phosphoribosylanthranilate transferase TC81895 BF051397 cLEM22D24 VIIIA12 T2B24 R1 C2 r4-c2 r1-c3 {Arabidopsis thaliana}GP|7267861|emb|CAB78204.1||AL starch phosphorylase (AA 1-966) {Solanum tuberosum} TC81900 BF097142 cLEW19F23 XIIE3 T3J6 R19 C10 r2-c1 r4-c3 contains similarity to cyclopropane fatty acid TC81904 AW616028 cTOA17L12 XVID11 T4H22 R3 C8 r2-c2 r1-c4 synthase~gene_id: MEE5.5 {Arabidopsis thaliana} PROBABLE VACUOLAR ATP SYNTHASE TC81929 BG134700 cTOE17L19 XVIIID6 T5G12 R13 C7 r3-c2 r4-c4 SUBUNIT F (EC 3.6.1.34) (V-ATPASE F SUBUNIT) (VACUOLAR PROTON PUMP F cytochrome P450-like protein {Arabidopsis TC81940 BE433060 cLEG12G7 VD11 T2G21 R4 C7 r4-c2 r1-c3 thaliana}GP|7270932|emb|CAB80611.1||AL161595 cytochrome P cytochrome P450-like protein {Arabidopsis TC81993 AW399577 cLPT8E17 XVIC3 T4F6 R19 C6 r2-c2 r1-c4 thaliana}PIR|T46196|T46196 cytochrome P450-like protein- uroporphyrinogen decarboxylase {Arabidopsis thaliana} TC81996 BG128715 cTOF21H22 XIXE4 T5J7 R18 C10 r3-c2 r4-c4 succinate dehydrogenase flavoprotein alpha subunit TC82029 BE434365 cLEG16B16 VE9 T2I17 R8 C9 r4-c2 r1-c3 {Arabidopsis thaliana}GP|8843734|dbj|BAA97282.1| HD-Zip protein {Arabidopsis TC82042 BG132703 cTOE8N13 XVIIIG5 T5M10 R15 C13 r3-c2 r4-c4 thaliana}GP|3132474|gb|AAC16263.1||AC003096 homeodomain transcription f phosphate transporter{circumflex over ( )}{circumflex over ( )}putative phosphate TC82044 AI781884 cLES17O18 XF6 T3K12 R13 C11 r2-c1 r4-c3 transporter{circumflex over ( )}{circumflex over ( )}inorganic phosphate transporter heat stress transcription factor A3 {Lycopersicon TC82048 AW034881 cLEC32C19 IH8 T1O15 R12 C15 r1-c2 r3-c3 peruvianum} putative glucosyl transferase {Arabidopsis TC82051 AW650919 cLEI14J16 XVIF5 T4L10 R15 C12 r2-c2 r1-c4 thaliana}PIR|H84784|H84784 probable glucosyl transferase contains similarity to chalcone-flavonone isomerase TC82093 BE435759 cLEG28N15 VH9 T2O17 R8 C15 r4-c2 r1-c3 (chalcone isomerase)~gene_id: K18I23.7 {Arabidops phosphoribosylanthranilate isomerase {Arabidopsis TC82095 BE435421 cLEG26N3 VG10 T2M19 R6 C13 r4-c2 r1-c3 thaliana} LIN6{circumflex over ( )}{circumflex over ( )}acid invertase TC82103 AW040329 cLET5E19 XIIB7 T3D14 R11 C4 r2-c1 r4-c3 Contains similarity to ARI, RING finger protein TC82118 AW624814 cLEZ8C12 XIVG6 T4M12 R13 C13 r2-c2 r1-c4 gb|X98309 from Drosophila melanogaster. ESTs gb|T44 transcription factor-like protein {Arabidopsis TC82130 AW039518 cLET14M13 XID8 T3H15 R12 C8 r2-c1 r4-c3 thaliana}GP|7576196|emb|CAB87947.1||AL163912 transcr polyphenol oxidase precursor TC82138 BF098557 cLEW27J20 XIIH7 T3P14 R11 C16 r2-c1 r4-c3 bHLH transcription factor GBOF-1 {Tulipa gesneriana} TC82153 BF050210 cLEML17A5 VIIG9 T2N17 R8 C14 r4-c2 r1-c3 glycerol-3-phosphate dehydrogenase {Arabidopsis TC82167 BF050313 cLEM17G22 VIE3 T2I6 R19 C9 r4-c2 r1-c3 thaliana}PIR|F84832|F84832 glycerol-3-phosphate deh putative cytochrome P450 {Oryza TC82169 AI488390 cLED21I12 IVA3 T1B6 R19 C2 r1-c2 r3-c3 sativa}GP|11761117|dbj|BAB19107.1||AP002839 putative cytochrome P45 transcription factor IIA small subunit {Arabidopsis TC82195 BG132223 cTOE6J10 XVIIIG1 T5M2 R23 C13 r3-c2 r4-c4 thaliana}GP|5051786|emb|CAB45079.1||AL078637 tr glucosyltransferase-like protein {Arabidopsis TC82199 AW623225 cTOB9O19 XVIIC2 T5E3 R22 C5 r3-c2 r4-c4 thaliana}GP|7340661|emb|CAB82941.1||AL162506 putative chalcone synthase-like protein {Arabidopsis TC82205 AW944832 cTOB12G4 XVIIA1 T5A1 R24 C1 r3-c2 r4-c4 thaliana}GP|7270436|emb|CAB80202.1||AL161586 chalcone s sugar transporter-like protein {Arabidopsis thaliana} TC82207 BG123226 cTOF1A20 XIXC10 T5F19 R6 C6 r3-c2 r4-c4 putative cytochrome P450 {Arabidopsis TC82226 AI898212 cLED32E24 IIIG1 T1N1 R24 C14 r1-c2 r3-c3 thaliana}GP|13877669|gb|AAK43912.1|AF370593_1|AF370593 putati putative zinc finger protein {Arabidopsis TC82243 AW032181 cLEC20K13 IE2 T1I3 R22 C9 r1-c2 r3-c3 thaliana}GP|7270045|emb|CAB79860.1||AL161579 putative zin 2-oxoglutarate/malate translocator precursor {Spinacia TC82252 BE437181 cLEG1G13 VF10 T2K19 R6 C11 r4-c2 r1-c3 oleracea}SP|Q41364|SOT1_SPIOL 2- OXOGLUTARATE NADH-dependent glutamate synthase {Arabidopsis TC82279 AW032148 cLEC38H15 IIC7 T1E14 R11 C5 r1-c2 r3-c3 thaliana} anthocyanidin 3-O-glucosyltransferase {Petunia x TC82331 BG628982 cLEL24M4 XXIA2 T6A3 R22 C1 r3-c1 r2-c4 hybrida} 3-methylcrotonyl-CoA carboxylase non-biotinylated TC82338 AW649104 cLEI7I13 VIIF11 T2L21 R4 C12 r4-c2 r1-c3 subunit {Arabidopsis thaliana}GP|7021224|gb|AAF35 cytochrome P450-like protein {Arabidopsis TC82348 AW033276 cLEC28N5 IG7 T1M13 R12 C13 r1-c2 r3-c3 thaliana}GP|7270098|emb|CAB79912.1||AL161580 Cytochrome P transketolase 1 {Capsicum TC82386 AW035937 cLEC37J10 IIC3 T1E6 R19 C5 r1-c2 r3-c3 annuum}PIR|T09541|T09541 transketolase (EC 2.2.1.1) TKT1 precursor, chlor HEAT SHOCK FACTOR PROTEIN 5 (HSF 5) (HEAT TC82389 BE459508 cLEM7C5 VIIIE10 T2J20 R5 C10 r4-c2 r1-c3 SHOCK TRANSCRIPTION FACTOR 5) (HSTF 5).GP|6624614|emb|CAB Similar to Populus balsamifera subsp. trichocarpa X TC82393 BG626572 cLEL13F1 XXIB8 T6C15 R12 C3 r3-c1 r2-c4 Populus deltoides vegetative storage protein. (L putative enolase (2-phospho-D-glycerate hydroylase) TC82394 BF112854 cLEG42J1 VIF8 T2K16 R9 C11 r4-c2 r1-c3 {Arabidopsis thaliana}PIR|G84697|G84697 hypothe putative CCCH-type zinc finger protein {Arabidopsis TC82395 AW649384 cLEI8G9 IVH9 T1P18 R7 C16 r1-c2 r3-c3 thaliana}PIR|D84581|D84581 probable CCCH-type z 3-dehydroquinate synthase-like protein {Arabidopsis TC82414 BE353857 cTOD6D17 XVIIIA1 T5A2 R23 C1 r3-c2 r4-c4 thaliana} cytochrome P450-like protein {Arabidopsis TC82416 AW738712 cTOD8E14 XVIIIA12 T5A24 R1 C1 r3-c2 r4-c4 thaliana}GP|7270932|emb|CAB80611.1||AL161595 cytochrome P isoflavone reductase homolog {Solanum TC82426 AI897693 cLED30K7 IIIF7 T1L13 R12 C12 r1-c2 r3-c3 tuberosum}SP|P52578|IFRH_SOLTU ISOFLAVONE REDUCTASE HOMOLOG ( putative pyrophosphate--fructose-6-phosphate 1- TC82429 AW929062 cTOC3P9 XIIIE2 T4I3 R22 C9 r2-c2 r1-c4 phosphotransferase {Arabidopsis thaliana}PIR|B84613| phosphoglycerate mutase {Solanum tuberosum} TC82433 AI777247 cLER20D8 XVIIF12 T5K23 R2 C11 r3-c2 r4-c4 6-phosphogluconate dehydrogenase, putative; 13029-14489 TC82459 BG125863 cTOF10K5 XVIIIG8 T5M16 R9 C13 r3-c2 r4-c4 {Arabidopsis thaliana} putative P-protein: chorismate mutase, prephenate TC82472 BG134235 cTOE15D14 XVIIIC9 T5E18 R7 C5 r3-c2 r4-c4 dehydratase {Arabidopsis thaliana} putative arginine methyltransferase {Arabidopsis TC82475 BF050261 cLEM17M11 XIVA2 T4A4 R21 C1 r2-c2 r1-c4 thaliana} P450 hydroxylase {Petunia x TC82490 AW035596 cLEC39N22 IID2 T1G4 R21 C7 r1-c2 r3-c3 hybrida}PIR|S32110|S32110 cytochrome P450 PET-1- garden petunia (fragm pathogenesis-related homeodomain protein (prhp) TC82493 BG135032 cTOE21I7 XVIIIE3 T5I6 R19 C9 r3-c2 r4-c4 {Petroselinum crispum}SP|P48786|PRH_PETCR PATHOGENE ferredoxin--nitrite reductase {Nicotiana TC82500 AW648617 cLEI5J9 XVIA10 T4B20 R5 C2 r2-c2 r1-c4 tabacum}GP|19893|emp|CAA46940.1||X66145 ferredoxin--nitrit contains similarity to heat shock transcription TC82508 AW649243 cLEI7H17 VIIF10 T2L19 R6 C12 r4-c2 r1-c3 factor~gene_id: MOB24.9 {Arabidopsis thaliana} starch synthase {Ipomoea batatas} TC82511 BG630199 cLEL33H7 XXIH10 T6O19 R6 C15 r3-c1 r2-c4 alpha-glucosidase {Solanum tuberosum subsp. TC82534 AW623694 cTOB11D18 XVIG1 T4N2 R23 C14 r2-c2 r1-c4 tuberosum} similar to class I knotted-like homeodomain protein TC82559 AW035887 cLEC35D19 IIB2 T1C4 R21 C3 r1-c2 r3-c3 (LeT6 putative internal rotenone-insensitive NADH TC82565 AI773904 cLER8F23 XC7 T3E14 R11 C5 r2-c1 r4-c3 dehydrogenase {Solanum tuberosum} putative C3HC4-type RING zinc finger protein TC82567 AI780031 cLES9N18 XIB9 T3D17 R8 C4 r2-c1 r4-c3 {Arabidopsis thaliana}GP|11908040|gb|AAG41449.1|AF3268 acetyl-CoA C-acetyltransferase {Arabidopsis thaliana} TC82576 BE458863 cLEM4F14 VIIID8 T2H16 R9 C8 r4-c2 r1-c3 amidophosphoribosyltransferase {Arabidopsis thaliana} TC82583 BE451488 cLEY18N18 XIH11 T3P21 R4 C16 r2-c1 r4-c3 putative anthocyanin 5-aromatic acyltransferase TC82613 AI775065 cLER14O11 IXF7 T3K13 R12 C11 r2-c1 r4-c3 {Arabidopsis thaliana}PIR|G84823|G84823 probable an cystathionine beta-lyase {Solanum tuberosum} TC82650 AI487273 cLED11M11 IIG12 T1M24 R1 C13 r1-c2 r3-c3 glutamine synthetase I {Medicago truncatula} TC82659 BG129068 cTOF23A10 XIXF6 T5L11 R14 C12 r3-c2 r4-c4 cTOF23A10 putative cytochrome P450; 1456-3294 {Arabidopsis TC82728 BF097238 cLEW19J16 XIIE7 T3J14 R11 C10 r2-c1 r4-c3 thaliana}GP|10092278|gb|AAG12691.1|AC025814_15| AC0 HOMEOBOX-LEUCINE ZIPPER PROTEIN HAT22 TC82731 AW222687 cLEN9E11 IXD12 T3G23 R2 C7 r2-c1 r4-c3 (HD-ZIP PROTEIN 22).GP|549887|gb|AAA56902.1||U09336 homeobox transcription factor inhibitor I kappa B homolog TC82775 AW160235 cLPT1I9 XVH8 T4P15 R12 C16 r2-c2 r1-c4 {Arabidopsis thaliana}GP|1773295|gb|AAC49611.1||U7 putative glycerol-3-phosphate dehydrogenase TC82784 BE354321 cTOD9P8 XVIIIB8 T5C16 R9 C3 r3-c2 r4-c4 {Arabidopsis thaliana} NADH dehydrogenase like protein {Arabidopsis TC82792 AW738592 cTOD7J8 XVIIIA7 T5A14 R11 C1 r3-c2 r4-c4 thaliana}GP|7268946|emb|CAB81256.1||AL161555 NADH dehy zinc finger protein SHI-like {Arabidopsis TC82801 AW034970 cLEC31N20 IH6 T1O11 R14 C15 r1-c2 r3-c3 thaliana}GP|4929803|gb|AAD34162.1|AF152555_1|AF152555 put inorganic phosphate transporter TC82826 AW622613 cLEX15D8 XIIIC10 T4E19 R6 C5 r2-c2 r1-c4 polyneuridine aldehyde esterase {Rauvolfia serpentina} TC82834 AI772823 cLER4A2 XB10 T3C20 R5 C3 r2-c1 r4-c3 alpha-glucosidase {Solanum tuberosum subsp. TC82868 AI487472 cLED11M2 IIH1 T1O2 R23 C15 r1-c2 r3-c3 tuberosum} ABC transporter-like protein {Arabidopsis TC82872 BF097895 cLEW24O17 XVC5 T4F9 R16 C6 r2-c2 r1-c4 thaliana}GP|13899119|gb|AAK48981.1|AF370554_1|AF370554 AB heat shock factor protein hsf24 (heat shock transcription TC82923 BG134658 cTOE17D21 XVIIID3 T5G6 R19 C7 r3-c2 r4-c4 factor 24) (hstf 24) (heat stress transcri sugar transporter like protein {Arabidopsis TC82942 BG137839 cLPP7D3 XVF2 T4L3 R22 C12 r2-c2 r1-c4 thaliana}GP|2464913|emb|CAB16808.1||Z99708 sugar transp cytochrome P450-like protein {Arabidopsis TC82954 AW621777 cLEX13E10 XIIIC1 T4E1 R24 C5 r2-c2 r1-c4 thaliana}PIR|T47554|T47554 cytochrome P450 homolog F8J2.1 TRYPTOPHAN SYNTHASE BETA CHAIN 2 TC82960 AW650635 cLEI13J17 VIIB12 T2D23 R2 C4 r4-c2 r1-c3 PRECURSOR (EC 4.2.1.20).GP|2792520|gb|AAB97087.1||AF042320 tryptop putative C3HC4-type RING zinc finger protein TC82965 AW034233 cLEC32P10 IH11 T1O21 R4 C15 r1-c2 r3-c3 {Arabidopsis thaliana}PIR|B84813|B84813 probable RING Similar to gb|Z84571 anthranilate N- TC82992 AW154873 cLEW1M9 XIIF9 T3L18 R7 C12 r2-c1 r4-c3 hydroxycinnamoyl/benzoyltransferase from Dianthus caryophyllus. ABC transporter homolog {Populus nigra} TC83000 AW035260 cLEC34N2 IIA12 T1A24 R1 C1 r1-c2 r3-c3 contains similarity to ABC TC83006 BG140588 cLPP17P7 XVE3 T4J5 R20 C10 r2-c2 r1-c4 transporter~gene_id: MAC9.4 {Arabidopsis thaliana} putative strictosidine synthase TC83008 BG627604 cLEL18I5 XXID6 T6G11 R14 C7 r3-c1 r2-c4 phosphate/phosphoenolpyruvate translocator precursor TC83014 AW040539 cLET6N24 XIIC1 T3F2 R23 C6 r2-c1 r4-c3 {Nicotiana tabacum}GP|1778145|gb|AAB40648.1||U putative enolase; 31277-33713 {Arabidopsis TC83066 AI488919 cLED18H15 IIIB8 T1D15 R12 C4 r1-c2 r3-c3 thaliana}PIR|B96768|B96768 protein enolase F2P9.10 [impo diacylglycerol kinase {Lycopersicon esculentum} TC83073 AW616611 cLHT11J12 XIVH8 T4O16 R9 C15 r2-c2 r1-c4 cytochrome P450 {Capsicum annuum} TC83085 BF097766 cLEW23F11 XIIG4 T3N8 R17 C14 r2-c1 r4-c3 contains similarity to RNA polymerase transcriptional TC83117 BG131064 cTOE2M8 XVIIIF4 T5K8 R17 C11 r3-c2 r4-c4 regulation mediator~gene_id: MHC9.3 {Arabidopsi acetyl-CoA synthetase, putative; 45051-31547 TC83139 BG124837 cTOF6J17 XXF3 T5L6 R19 C12 r3-c2 r4-c4 {Arabidopsis thaliana}PIR|D96595|D96595 probable acety ABC transporter-like protein {Arabidopsis TC83143 AW035264 cLEC34L14 IIA10 T1A20 R5 C1 r1-c2 r3-c3 thaliana}PIR|T07717|T07717 probable ABC-type transport pr putative sugar transporter {Arabidopsis thaliana} TC83157 AW032681 cLEC25N4 IF12 T1K23 R2 C11 r1-c2 r3-c3 putative zinc finger protein {Arabidopsis TC83165 BE432483 cLEG8M16 VIIA1 T2B1 R24 C2 r4-c2 r1-c3 thaliana}GP|7270045|emb|CAB79860.1||AL161579 putative zin CYTOCHROME P450 98A2 (EC 1.14.—.—). TC83207 BE432077 cLEG5C20 VIH3 T2O6 R19 C15 r4-c2 r1-c3 GP|2738998|gb|AAB94587.1||AF022458 CYP98A2p {Glycine max}PIR|T0 transcription factor, putative {Arabidopsis TC83217 BF051437 cLEM22N8 VIIIB7 T2D14 R11 C4 r4-c2 r1-c3 thaliana}PIR|E96612|E96612 probable transcription facto auxin-induced basic helix-loop-helix transcription factor TC83218 BG129020 cTOF23G15 XIXF10 T5L19 R6 C12 r3-c2 r4-c4 {Gossypium hirsutum} ABC transporter-like protein {Arabidopsis TC83254 BE460242 cLEG27H11 VH1 T2O1 R24 C15 r4-c2 r1-c3 thaliana}GP|9964121|gb|AAG09829.1|AF287699_1|AF287699 hal bHLH transcription factor JAF13 {Petunia x hybrida} TC83264 BE435307 cLEG25N14 VG9 T2M17 R8 C13 r4-c2 r1-c3 glycerol-3-phosphate dehydrogenase {Arabidopsis TC83308 AI778474 cLES5M24 XH12 T3O24 R1 C15 r2-c1 r4-c3 thaliana}PIR|F84832|F84832 glycerol-3-phosphate deh cytochrome p450 1xxia3 {Solanum TC83334 BG734604 cLEL12A1 XXIB4 T6C7 R18 C3 r3-c1 r2-c4 melongena}SP|P37119|C713_SOLME CYTOCHROME P450 71A3 (EC 1.14.—.—) ( putative 6-phosphogluconolactonase {Arabidopsis TC83350 BE451183 cLEY16L2 XIG4 T3N7 R18 C14 r2-c1 r4-c3 thaliana} soluble starch (bacterial glycogen) synthase {Solanum TC83359 BE434446 cLEG17G1 VF4 T2K7 R18 C11 r4-c2 r1-c3 tuberosum}SP|P93568|UGS2_SOLTU SOLUBLE GLYCOG beta-amylase-like {Arabidopsis thaliana} TC83371 AW648284 cLEI4E17 VIIE5 T2J9 R16 C10 r4-c2 r1-c3 cytochrome P450 {Arabidopsis TC83399 AW031490 cLEC40I14 IID6 T1G12 R13 C7 r1-c2 r3-c3 thaliana}GP|7268718|emb|CAB78925.1||AL161550 cytochrome P450 {Arabidop fructokinase {Lycopersicon TC83425 BG139723 cLPP14E5 XVD10 T4H19 R6 C8 r2-c2 r1-c4 esculentum}GP|2102691|gb|AAB57733.1||U64817 fructokinase {Lycopersicon e putative citrate synthase {Arabidopsis TC83487 AW037360 cLET1C16 XIE6 T3J11 R14 C10 r2-c1 r4-c3 thaliana}PIR|C84858|C84858 probable citrate synthase [import putative acetone-cyanohydrin lyase {Arabidopsis TC83491 BE450272 cLEY12P15 XIIIG1 T4M1 R24 C13 r2-c2 r1-c4 thaliana}PIR|T01151|T01151 probable acetone-cyanohy putative pyrophosphate-dependent phosphofructo-1- TC83500 AW616742 cLHT12F16 XIIF8 T3L16 R9 C12 r2-c1 r4-c3 kinase {Arabidopsis thaliana} uroporphyrinogen decarboxylase {Arabidopsis thaliana} TC83506 AI491153 cLEB3I24 IB5 T1C9 R16 C3 r1-c2 r3-c3 Zn finger protein {Nicotiana TC83522 AI490285 cLED24N8 IIID2 T1H3 R22 C8 r1-c2 r3-c3 tabacum}GP|1360078|emb|CAA66601.1||X97942 Zn finger protein {Nicotiana transcription factor WRKY6 {Arabidopsis TC83553 AW648696 cLEI5A6 VIIE10 T2J19 R6 C10 r4-c2 r1-c3 thaliana}GP|12658412|gb|AAK01128.1|AF331713_1|AF331713 tran limonene cyclase like protein {Arabidopsis TC83555 AI488634 cLED17P22 IIIB5 T1D9 R16 C4 r1-c2 r3-c3 thaliana}GP|2245029|emb|CAB10449.1||Z97341 limonene cycl GMP synthase; 61700-64653 {Arabidopsis TC83694 AW616602 cLHT11H10 XIVH4 T4O8 R17 C15 r2-c2 r1-c4 thaliana}PIR|E96661|E96661 GMP synthase, 61700-64653 [import beta-amylase {Glycine TC83696 BG125052 cTOF7D1 XXF6 T5L12 R13 C12 r3-c2 r4-c4 max}GP|902938|dbj|BAA09462.1||D50866 beta- amylase {Glycine max} pyruvate kinase (EC 2.7.1.40) A, chloroplast-common TC83701 AI780946 cLES13J24 XD10 T3G20 R5 C7 r2-c1 r4-c3 tobacco cytochrome p450-like protein {Arabidopsis TC83712 AW617482 cLHT23O11 XVB3 T4D5 R20 C4 r2-c2 r1-c4 thaliana}GP|7270718|emb|CAB80401.1||AL161591 cytochrome p Putative UDP-glucose glucosyltransferase {Arabidopsis TC83719 AI482910 cLEB1J8 IA6 T1A11 R14 C1 r1-c2 r3-c3 thaliana}PIR|H86356|H86356 probable UDP-gluco Similar to gb|Z84386 anthranilate N- TC83737 AW616931 cLHT18F9 XVA6 T4B11 R14 C2 r2-c2 r1-c4 hydroxycinnamoyl/benzoyltransferase from Dianthus caryophyllus. Phosphoglycerate dehydrogenase-like protein TC83740 AW650818 cLEI14F1 VIIC2 T2F3 R22 C6 r4-c2 r1-c3 {Arabidopsis thaliana}GP|7270370|emb|CAB80137.1||AL1615 phosphoribosyl pyrophosphate synthase isozyme 4 TC83753 AW623664 cTOB11N7 XVIG7 T4N14 R11 C14 r2-c2 r1-c4 {Spinacia oleracea} putative dihydroflavonol reductase {Oryza sativa} TC83761 AW624036 cTOB13L22 XVIH9 T4P18 R7 C16 r2-c2 r1-c4 hexose transporter TC83763 tyrosine/dopa decarboxylase {Thalictrum flavum subsp. TC83804 BE449262 cLHT31C18 XVB12 T4D23 R2 C4 r2-c2 r1-c4 glaucum} Cytochrom P450-like protein {Arabidopsis TC83813 BF096935 cLEW18E10 XIID12 T3H24 R1 C8 r2-c1 r4-c3 thaliana}PIR|T46159|T46159 cytochrome P450-like protein- glycolate oxidase {Arabidopsis thaliana} TC83832 BE449243 cLHT31O9 XVC4 T4F7 R18 C6 r2-c2 r1-c4 alpha-glucan phosphorylase, h isozyme phosphorylase TC83865 BG734793 cLEL16K20 XXID7 T6G13 R12 C7 r3-c1 r2-c4 h) {Solanum tuberosum}SP|P32811|PHSH_SOLTU ALPH CYTOCHROME P450 98A3 (EC 1.14.—.—). TC83866 AI779624 cLES8L1 XIB1 T3D1 R24 C4 r2-c1 r4-c3 GP|2623303|gb|AAB86449.1||AC002409 putative cytochrome P450 {Ara general negative transcription regulator-like TC83872 BG140293 cLPP16F4 XVE1 T4J1 R24 C10 r2-c2 r1-c4 {Arabidopsis thaliana} Dof zinc finger protein {Nicotiana TC83881 AI487752 cLED11A23 IIG5 T1M10 R15 C13 r1-c2 r3-c3 tabacum}PIR|T02203|T02203 finger protein Dof- common tobacco (f putative ABC transporter {Arabidopsis TC83901 AI779502 cLES8O5 XIB6 T3D11 R14 C4 r2-c1 r4-c3 thaliana}GP|4115931|gb|AAD03441.1||AF118223 contains similari ornithine carbamoyltransferase; OCTase {Canavalia TC83905 AI778009 cLES3P1 XH4 T3O8 R17 C15 r2-c1 r4-c3 lineata}GP|12003188|gb|AAG43481.1|AF203688_1|AF20 succinate dehydrogenase iron-protein subunit TC83937 AW032637 cLEC20L4 IE3 T1I5 R20 C9 r1-c2 r3-c3 {Arabidopsis thaliana} tyrosine aminotransferase {Arabidopsis thaliana} TC83980 AW219060 cLEX2J17 XIIID8 T4G15 R12 C7 r2-c2 r1-c4 ferredoxin--nitrite reductase {Nicotiana TC83986 AI776535 cLER18J6 IXH8 T3O15 R12 C15 r2-c1 r4-c3 tabacum}GP|861067|emb|CAA46942.1||X66147 ferredoxin--nitri legumin-like protein {Arabidopsis TC84014 AW622321 cLEX14L6 XIIIC8 T4E15 R12 C5 r2-c2 r1-c4 thaliana}PIR|H84687|H84687 legumin-like protein [imported]- Arab MADS transcriptional factor; STMADS16 {Solanum TC84038 AI482813 cLEB3L11 IB6 T1C11 R14 C3 r1-c2 r3-c3 tuberosum}PIR|T06995|T06995 probable MADS box transc amidophosphoribosyltransferase {Arabidopsis thaliana} TC84044 AW154806 cLEW1C23 XIIE11 T3J22 R3 C10 r2-c1 r4-c3 transketolase 1 {Capsicum TC84048 BE450953 cLEY15H24 XIIIH5 T4O9 R16 C15 r2-c2 r1-c4 annuum}PIR|T09541|T09541 transketolase (EC 2.2.1.1) TKT1 precursor, chlor UDP-GLUCOSE 4-EPIMERASE GEPI48 (EC 5.1.3.2) TC84055 AI484890 cLED3N7 IVA4 T1B8 R17 C2 r1-c2 r3-c3 (GALACTOWALDENASE) (UDP-GALACTOSE 4- EPIMERASE).GP|3021 contains similarity to chorismate mutase-T and TC84057 AW616637 cLHT11N22 XIVH11 T4O22 R3 C15 r2-c2 r1-c4 prephenate dehydrogenase~gene_id: MGG23.1 {Arabidopsis Strong similarity to gb|Z50851 HD-zip (athb-8) gene TC84068 AI781675 cLES16B20 XE6 T3I12 R13 C9 r2-c1 r4-c3 from Arabidopsis thaliana containing Homeobox PF Is a member of the PF|00044 glyceraldehyde 3- TC84078 AW930283 cLEF41H8 IVF3 T1L6 R19 C12 r1-c2 r3-c3 phosphate dehydrogenase family. ESTs gb|T43985, gb|N38 putative hydroxymethylglutaryl-CoA lyase TC84085 AW650521 cLEI13C14 VIIB7 T2D13 R12 C4 r4-c2 r1-c3 {Arabidopsis thaliana}PIR|T02655|T02655 hydroxymethylgluta putative anthranilate N- TC84103 AW217721 cTOC6C19 XVIIE5 T5I9 R16 C9 r3-c2 r4-c4 hydroxycinnamoyl/benzoyltransferase {Arabidopsis thaliana}PIR|T00527|T00527 RING zinc finger protein-like {Arabidopsis thaliana} TC84140 AW222126 cLEN7C15 IXD4 T3G7 R18 C7 r2-c1 r4-c3 CCAAT box binding factor/transcription factor Hap2a TC84198 AW030886 cLEC15K2 ID7 T1G13 R12 C7 r1-c2 r3-c3 {Arabidopsis thaliana}PIR|T49898|T49898 CCAAT MADS-box transcription factor FBP24 {Petunia x TC84232 AI899235 cLED37P16 IIIH4 T1P7 R18 C16 r1-c2 r3-c3 hybrida} adenylosuccinate lyase-like protein; 104558-106845 TC84319 BF097158 cLEW19J11 XIIE6 T3J12 R13 C10 r2-c1 r4-c3 {Arabidopsis thaliana}PIR|B86484|B86484 hypothet pyruvate kinase-like protein {Arabidopsis TC84320 AW037759 cLET3L18 XIH9 T3P17 R8 C16 r2-c1 r4-c3 thaliana}PIR|T47556|T47556 pyruvate kinase-like protein- unnamed protein product TC84322 AW040240 cLET19N8 XIE3 T3J5 R20 C10 r2-c1 r4-c3 {unidentified}GP|2462911|emb|CAB06081.1||Z83832 UDP-glucose:sterol glucosyl folylpolyglutamate synthase-like protein {Arabidopsis TC84330 AI782088 cLES18G17 XF9 T3K18 R7 C11 r2-c1 r4-c3 thaliana} dihydroxy-acid dehydratase {Arabidopsis thaliana} TC84340 AI898180 cLED31P20 IIIF11 T1L21 R4 C12 r1-c2 r3-c3 CTP synthase like protein {Arabidopsis TC84368 AW979649 cLEW8A16 XIIH10 T3P20 R5 C16 r2-c1 r4-c3 thaliana}GP|7268827|emb|CAB79032.1||AL161552 CTP synthase 1i Putative acyl-CoA:1-acylglycerol-3-phosphate TC84467 AA824736 CT041 XVIC7 T4F14 R11 C6 r2-c2 r1-c4 acyltransferase {Arabidopsis thaliana}PIR|D96550|D965 putative gluconokinase {Arabidopsis TC84507 AI781650 cLES16N11 XF1 T3K2 R23 C11 r2-c1 r4-c3 thaliana}PIR|C84544|C84544 probable gluconokinase [imported]- Strong similarity to F19I3.2 GP|3033375 putative TC84522 AI491197 cLEB1G24 IA3 T1A5 R20 C1 r1-c2 r3-c3 berberine bridge enzyme from Arabidapsis thaliana B homeodomain-leucine zipper protein 57 {Glycine max} TC84550 AW617989 cLPT11L19 XVF12 T4L23 R2 C12 r2-c2 r1-c4 transcription factor {Nicotiana tabacum} TC84557 AW933661 cLEF55M14 VB12 T2C23 R2 C3 r4-c2 r1-c3 carbamoyl-phosphate synthetase small subunit TC84578 AW092546 cLET20F12 XIE11 T3J21 R4 C10 r2-c1 r4-c3 {Arabidopsis thaliana} UDP glucose dehydrogenase 108 A1 T6B1 R24 C2 r3-c1 r2-c4 GDP mannose pyrophosphorylase 110 A2 T6B3 R22 C2 r3-c1 r2-c4 β galactosidase 112 A3 T6B5 R20 C2 r3-c1 r2-c4 Sucrose phosphate synthase 116 A4 T6B7 R18 C2 r3-c1 r2-c4 Laccase 122 A5 T6B9 R16 C2 r3-c1 r2-c4 Oxoglutarate malate translocator 130 A6 T6B11 R14 C2 r3-c1 r2-c4 Uncoupling protein 136 A7 T6B13 R12 C2 r3-c1 r2-c4 unknown funktion 167 A8 T6B15 R12 C2 r3-c1 r2-c4 unknown funktion 168 A9 T6B17 R8 C2 r3-c1 r2-c4 beta-amylase 169 A10 T6B19 R6 C2 r3-c1 r2-c4 alpha-amylase 1 170 A11 T6B21 R4 C2 r3-c1 r2-c4 alpha-amylase 2 171 A12 T6B23 R2 C2 r3-c1 r2-c4 alpha-glucosidase 11 172 B1 T6D1 R24 C4 r3-c1 r2-c4 alpha-glucosidase 19 173 B2 T6D3 R22 C4 r3-c1 r2-c4 Branching enzyme 174 B3 T6D5 R20 C4 r3-c1 r2-c4 ATPase 195 B4 T6D7 R18 C4 r3-c1 r2-c4 Adenylate kinase 204 B5 T6D9 R16 C4 r3-c1 r2-c4 UMP-synthase 211 B6 T6D11 R14 C4 r3-c1 r2-c4 Major intrinsic protein 1 218 B7 T6D13 R12 C4 r3-c1 r2-c4 Major intrinsic protein 2 226 B8 T6D15 R12 C4 r3-c1 r2-c4 Phosphate transporter 1 229 B9 T6D17 R8 C4 r3-c1 r2-c4 Phosphate transporter 2 230 B10 T6D19 R6 C4 r3-c1 r2-c4 Phosphate transporter 3 231 B11 T6D21 R4 C4 r3-c1 r2-c4 Disproporting enzyme 239 B12 T6D23 R2 C4 r3-c1 r2-c4 Branching enzyme 261 C1 T6F1 R24 C6 r3-c1 r2-c4 Starch phosphorylase, plastidic 265 C2 T6F3 R22 C6 r3-c1 r2-c4 Starch phosphorylase, cytosolic 266 C3 T6F5 R20 C6 r3-c1 r2-c4 Granule bound starch synthase 270 C4 T6F7 R18 C6 r3-c1 r2-c4 Root-phosphate-translocator 272 C5 T6F9 R16 C6 r3-c1 r2-c4 Potato-brittle-transporter1 274 C6 T6F11 R14 C6 r3-c1 r2-c4 Pyruvate kinase, cytosolic 300 C7 T6F13 R12 C6 r3-c1 r2-c4 Ppi:fru-6-P-phosphotransferase 301 C8 T6F15 R12 C6 r3-c1 r2-c4 Tonoplasts bound pyrophosphatase 302 C9 T6F17 R8 C6 r3-c1 r2-c4 Invertase, vacuolar 303 C10 T6F19 R6 C6 r3-c1 r2-c4 358 C11 T6F21 R4 C6 r3-c1 r2-c4 359 C12 T6F23 R2 C6 r3-c1 r2-c4 360 D1 T6H1 R24 C8 r3-c1 r2-c4 362 D2 T6H3 R22 C8 r3-c1 r2-c4 364 D3 T6H5 R20 C8 r3-c1 r2-c4 378 D4 T6H7 R18 C8 r3-c1 r2-c4 Glycogene synthase kinase 526 D5 T6H9 R16 C8 r3-c1 r2-c4 Amylogenine 533 D6 T6H11 R14 C8 r3-c1 r2-c4 Starch synthase I 534 D7 T6H13 R12 C8 r3-c1 r2-c4 Starch synthase II 535 D8 T6H15 R12 C8 r3-c1 r2-c4 Phosphoglycerate mutase 541 D9 T6H17 R8 C8 r3-c1 r2-c4 Hexokinase 595 D10 T6H19 R6 C8 r3-c1 r2-c4 D11 T6H21 R4 C8 r3-c1 r2-c4 Phosphoglucomutase 612 D12 T6H23 R2 C8 r3-c1 r2-c4 Phosphoglucomutase 615 E1 T6J1 R24 C10 r3-c1 r2-c4 Putative 14-3-3, unknown function 1054 E2 T6J3 R22 C10 r3-c1 r2-c4 Putative 14-3-3, unknown function 1055 E3 T6J5 R20 C10 r3-c1 r2-c4 Acid phosphate 1378 E4 T6J7 R18 C10 r3-c1 r2-c4 unknown funktion 1379 E5 T6J9 R16 C10 r3-c1 r2-c4 1480 E6 T6J11 R14 C10 r3-c1 r2-c4 1480 E7 T6J13 R12 C10 r3-c1 r2-c4 1513 E8 T6J15 R12 C10 r3-c1 r2-c4 beta-amylase 1681 E9 T6J17 R8 C10 r3-c1 r2-c4 unknown funktion 1685 E10 T6J19 R6 C10 r3-c1 r2-c4 Putativ starch degrading 1735 E11 T6J21 R4 C10 r3-c1 r2-c4 Putativ starch degrading 1737 E12 T6J23 R2 C10 r3-c1 r2-c4 ATP-sulfurylase, plastidic 1823 F1 T6L1 R24 C12 r3-c1 r2-c4 ATP-sulfurylase, cytosolic 1824 F2 T6L3 R22 C12 r3-c1 r2-c4 R1 protein 1894 F3 T6L5 R20 C12 r3-c1 r2-c4 KST#8-1 1907 F4 T6L7 R18 C12 r3-c1 r2-c4 ICDH-1 1908 F5 T6L9 R16 C12 r3-c1 r2-c4 StIPS-1 1909 F6 T6L11 R14 C12 r3-c1 r2-c4 Mips 1910 F7 T6L13 R12 C12 r3-c1 r2-c4 Malat-Enzym 1911 F8 T6L15 R12 C12 r3-c1 r2-c4 Aconitase 1937 F9 T6L17 R8 C12 r3-c1 r2-c4 1939 F10 T6L19 R6 C12 r3-c1 r2-c4 1940 F11 T6L21 R4 C12 r3-c1 r2-c4 1941 F12 T6L23 R2 C12 r3-c1 r2-c4 1942 G1 T6N1 R24 C14 r3-c1 r2-c4 1943 G2 T6N3 R22 C14 r3-c1 r2-c4 unknown funktion 1944 G3 T6N5 R20 C14 r3-c1 r2-c4 60S ribosomal protein L31 1945 G4 T6N7 R18 C14 r3-c1 r2-c4 Putative Lysopholipase 1946 G5 T6N9 R16 C14 r3-c1 r2-c4 unknown funktion 1947 G6 T6N11 R14 C14 r3-c1 r2-c4 unknown funktion 1948 G7 T6N13 R12 C14 r3-c1 r2-c4 unknown funktion 1949 G8 T6N15 R12 C14 r3-c1 r2-c4 3-phosphoshikimate 1-carboxyvinyltransferase 1951 G9 T6N17 R8 C14 r3-c1 r2-c4 homology to an unknown protein of Arabidopsis 1952 G10 T6N19 R6 C14 r3-c1 r2-c4 Ribisco small chain 2A precursor 1953 G11 T6N21 R4 C14 r3-c1 r2-c4 Isoamylase 1956 G12 T6N23 R2 C14 r3-c1 r2-c4 Fructokinase 1957 H1 T6P1 R24 C16 r3-c1 r2-c4 stearoyl-acyl carrier prot 1958 H2 T6P3 R22 C16 r3-c1 r2-c4 β-tubulin 1959 H3 T6P5 R20 C16 r3-c1 r2-c4 S-adenosylmethionin decarboxylase 1960 H4 T6P7 R18 C16 r3-c1 r2-c4 glucosidase 1961 H5 T6P9 R16 C16 r3-c1 r2-c4 tuberisation induced gene (DC 10) 1962 H6 T6P11 R14 C16 r3-c1 r2-c4 tuberisation induced gene (DC 8) 1963 H7 T6P13 R12 C16 r3-c1 r2-c4 tuberisation-related gene 1964 H8 T6P15 R12 C16 r3-c1 r2-c4 NtSUT1 1979 H9 T6P17 R8 C16 r3-c1 r2-c4 shaggy kinase 1980 H10 T6P19 R6 C16 r3-c1 r2-c4 bZIP DANN binding protein 1981 H11 T6P21 R4 C16 r3-c1 r2-c4 pollen specific ascorbat oxidase 1982 H12 T6P23 R2 C16 r3-c1 r2-c4 

1. A method for determining the function of a gene comprising (a) determining the amount of transcript for each of a set of candidate genes in two or more samples from an organism, wherein the samples correspond to different phenotypic and/or genotypic states of said organism; (b) determining the amount of each of a plurality of metabolites present in two or more samples corresponding to the same states as in (a); (c) analysing by suitable mathematical methods the data obtained in steps (a) and (b) in order to identify a transcript and at least one metabolite the amounts of which significantly correlate in the different states, said transcript corresponding to a gene having a function that influences the amount of said metabolite(s) in said organism.
 2. The method of claim 1, wherein the analysis in step (c) comprises the steps (i) determining transcripts the amount of which differs significantly between the samples of (a); and (ii) determining metabolites the amount of which differs significantly between the samples of (b); wherein the data obtained for the transcripts and the metabolites determined in steps (i) and (ii), respectively, are analysed by suitable mathematical methods in order to identify said transcript and metabolite(s) the amounts of which significantly correlate in the different states.
 3. The method of claim 1, wherein said gene encodes an enzyme, a regulatory protein, a transport protein or a transcription factor.
 4. The method of claim 1, wherein a set of at least 100 candidate genes is used in step (a).
 5. The method of claim 1, wherein probes that are homologous with respect to said organism are used for determining the amount of transcripts.
 6. The method of claim 1, wherein the different phenotypic and/or genotypic states are different developmental stages, taxonomic units, wild-type and mutant or transgenic organisms, infected and uninfected states, diseased and healthy states or different stages of a pathogenicity.
 7. The method of claim 1, wherein the amount of transcripts and the amount of metabolites is each determined from the same sample.
 8. The method of claim 1, wherein the metabolites comprise sugars, sugars alcohols, organic acids, amino acids, ascorbate, tocopherol, fatty acids, vitamins and/or polyamines.
 9. The method of claim 1, wherein at least 50 metabolites are determined in step (b).
 10. A method for identifying a gene which is capable of modifying the amount of a metabolite in an organism comprising steps (a) to (c) of the method of claim 1, wherein said transcript identified in step (c) corresponds to a gene being capable of modifying the amount of said metabolite(s) identified in step (c).
 11. A method for identifying a metabolite which is capable of modifying the amount of a transcript in an organism comprising steps (a) to (c) of the method of claim 1, wherein a metabolite identified in step (c) is a candidate for a metabolite being capable of modifying the amount of said transcript identified in step (c). 12-14. (canceled) 